Tricyclic compounds and methods of making and using same

ABSTRACT

The invention provides tricyclic compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tricyclic compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a national stage filing of PCT/US2011/044864 filed Jul. 21, 2011, which claims priority to U.S. Provisional Patent Application 61/366,650 filed Jul. 22, 2010 and U.S. Provisional Patent Application 61/470,093 filed Mar. 31, 2011, all of which are hereby incorporated by reference in their entirety.

BACKGROUND

Over 1.1 billion people worldwide are reported to be overweight. Obesity is estimated to affect over 90 million people in the United States alone. Twenty-five percent of the population in the United States over the age of twenty is considered clinically obese. While being overweight or obese presents problems (for example restriction of mobility, discomfort in tight spaces such as theater or airplane seats, social difficulties, etc.), these conditions, in particular clinical obesity, affect other aspects of health, i.e., diseases and other adverse health conditions associated with, exacerbated by, or precipitated by being overweight or obese. The estimated mortality from obesity-related conditions in the United States is over 300,000 annually (O'Brien et al. Amer J Surgery (2002) 184:4 S-8S; and Hill et al. (1998) Science, 280:1371).

There is no curative treatment for being overweight or obese. Traditional pharmacotherapies for treating an overweight or obese subject, such as serotonin and noradrenergic re-uptake inhibitors, noradrenergic re-uptake inhibitors, selective serotonin re-uptake inhibitors, intestinal lipase inhibitors, or surgeries such as stomach stapling or gastric banding, have been shown to provide minimal short-term benefits or significant rates of relapse, and have further shown harmful side-effects to patients.

MetAP2 encodes a protein that functions at least in part by enzymatically removing the amino terminal methionine residue from certain newly translated proteins such as glyceraldehyde-3-phosphate dehydrogenase (Warder et al. (2008) J Proteome Res 7:4807). Increased expression of the MetAP2 gene has been historically associated with various forms of cancer. Molecules inhibiting the enzymatic activity of MetAP2 have been identified and have been explored for their utility in the treatment of various tumor types (Wang et al. (2003) Cancer Res. 63:7861) and infectious diseases such as microsporidiosis, leishmaniasis, and malaria (Zhang et al. (2002) J. Biomed. Sci. 9:34). Notably, inhibition of MetAP2 activity in obese and obese-diabetic animals leads to a reduction in body weight in part by increasing the oxidation of fat and in part by reducing the consumption of food (Rupnick et al. (2002) Proc. Natl. Acad. Sci. USA 99:10730).

Such MetAP2 inhibitors may be useful as well for patients with excess adiposity and conditions related to adiposity including type 2 diabetes, hepatic steatosis, and cardiovascular disease (via e.g. ameliorating insulin resistance, reducing hepatic lipid content, and reducing cardiac workload). Accordingly, compounds capable of modulating MetAP2 are needed to address the treatment of obesity and related diseases as well as other ailments favorably responsive to MetAP2 modulator treatment.

SUMMARY

The invention provides, for example, compounds which may be modulators of MetAP2, and their use as medicinal agents, processes for their preparation, and pharmaceutical compositions containing them as an active ingredient both alone or in combination with other agents, as well as provides for their use as medicaments and/or in the manufacture of medicaments for the inhibition of MetAP2 activity in warm-blooded animals such as humans. In particular this invention relates to compounds useful for the treatment of obesity, type 2 diabetes, and other obesity-associated conditions. Also provided are pharmaceutical compositions comprising at least one disclosed compound and a pharmaceutically acceptable carrier.

In an embodiment, provided herein are compounds represented by formula I:

or pharmaceutically acceptable salts, stereoisomers, esters or prodrugs thereof, where A, B, D, E, R^(A1), R^(A2), Y, X, and n are as defined herein.

DETAILED DESCRIPTION

The features and other details of the disclosure will now be more particularly described. Before further description of the present invention, certain terms employed in the specification, examples and appended claims are collected here. These definitions should be read in light of the remainder of the disclosure and as understood by a person of skill in the art. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by a person of ordinary skill in the art.

Definitions

“Treating” includes any effect, e.g., lessening, reducing, modulating, or eliminating, that results in the improvement of the condition, disease, disorder and the like.

The term “alkenyl” as used herein refers to an unsaturated straight or branched hydrocarbon having at least one carbon-carbon double bond. Exemplary alkenyl groups include, but are not limited to, a straight or branched group of 2-6 or 3-4 carbon atoms, referred to herein as C₂₋₆alkenyl, and C₃₋₄alkenyl, respectively. Exemplary alkenyl groups include, but are not limited to, vinyl, allyl, butenyl, pentenyl, etc.

The term “alkoxy” as used herein refers to a straight or branched alkyl group attached to oxygen (alkyl-O—). Exemplary alkoxy groups include, but are not limited to, alkoxys of 1-6 or 2-6 carbon atoms, referred to herein as C₁₋₆alkoxy, and C₂₋₆alkoxy, respectively. Exemplary alkoxy groups include, but are not limited to methoxy, ethoxy, isopropoxy, etc.

The term “alkoxyalkyl” as used herein refers to a straight or branched alkyl group attached to oxygen, attached to a second straight or branched alkyl group (alkyl-O-alkyl-). Exemplary alkoxyalkyl groups include, but are not limited to, alkoxyalkyl groups in which each of the alkyl groups independently contains 1-6 carbon atoms, referred to herein as C₁₋₆alkoxy-C₁₋₆alkyl. Exemplary alkoxyalkyl groups include, but are not limited to methoxymethyl, 2-methoxyethyl, 1-methoxyethyl, 2-methoxypropyl, ethoxymethyl, isopropoxyethyl etc.

The term “alkyoxycarbonyl” as used herein refers to a straight or branched alkyl group attached to oxygen, attached to a carbonyl group (alkyl-O—C(O)—). Exemplary alkoxycarbonyl groups include, but are not limited to, alkoxycarbonyl groups of 1-6 carbon atoms, referred to herein as C₁₋₆alkoxycarbonyl. Exemplary alkoxycarbonyl groups include, but are not limited to, methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl, etc.

The term “alkenyloxy” used herein refers to a straight or branched alkenyl group attached to oxygen (alkenyl-O—). Exemplary alkenyloxy groups include, but are not limited to, groups with an alkenyl group of 3-6 carbon atoms, referred to herein as C₃₋₆alkenyloxy. Exemplary “alkenyloxy” groups include, but are not limited to allyloxy, butenyloxy, etc.

The term “alkynyloxy” used herein refers to a straight or branched alkynyl group attached to oxygen (alkynyl-O). Exemplary alkynyloxy groups include, but are not limited to, groups with an alkynyl group of 3-6 carbon atoms, referred to herein as C₃₋₆alkynyloxy. Exemplary alkynyloxy groups include, but are not limited to, propynyloxy, butynyloxy, etc.

The term “alkyl” as used herein refers to a saturated straight or branched hydrocarbon. Exemplary alkyl groups include, but are not limited to, straight or branched hydrocarbons of 1-6, 1-4, or 1-3 carbon atoms, referred to herein as C₁₋₆alkyl, C₁₋₄alkyl, and C₁₋₃alkyl, respectively. Exemplary alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, 2-methyl-1-butyl, 3-methyl-2-butyl, 2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl, isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, etc.

The term “alkylcarbonyl” as used herein refers to a straight or branched alkyl group attached to a carbonyl group (alkyl-C(O)—). Exemplary alkylcarbonyl groups include, but are not limited to, alkylcarbonyl groups of 1-6 atoms, referred to herein as C₁₋₆alkylcarbonyl groups. Exemplary alkylcarbonyl groups include, but are not limited to, acetyl, propanoyl, isopropanoyl, butanoyl, etc.

The term “alkynyl” as used herein refers to an unsaturated straight or branched hydrocarbon having at least one carbon-carbon triple bond. Exemplary alkynyl groups include, but are not limited to, straight or branched group of 2-6, or 3-6 carbon atoms, referred to herein as C₂₋₆alkynyl, and C₃₋₆alkynyl, respectively. Exemplary alkynyl groups include, but are not limited to, ethynyl, propynyl, butynyl, pentynyl, hexynyl, methylpropynyl, etc.

The term “carbonyl” as used herein refers to the radical —C(O)—.

The term “cyano” as used herein refers to the radical —CN.

The term “cycloalkoxy” as used herein refers to a cycloalkyl group attached to oxygen (cycloalkyl-O—). Exemplary cycloalkoxy groups include, but are not limited to, cycloalkoxy groups of 3-6 carbon atoms, referred to herein as C₃₋₆cycloalkoxy groups. Exemplary cycloalkoxy groups include, but are not limited to, cyclopropoxy, cyclobutoxy, cyclohexyloxy, etc.

The term “cycloalkyl” as used herein refers to a saturated or partially unsaturated hydrocarbon group of, for example, 3-6, or 4-6 carbons, referred to herein as C₃₋₆cycloalkyl or C₄₋₆cycloalkyl, respectively. Exemplary cycloalkyl groups include, but are not limited to, cyclohexyl, cyclopentyl, cyclopentenyl, cyclobutyl or cyclopropyl.

The terms “halo” or “halogen” as used herein refer to F, Cl, Br, or I.

The terms “heteroaryl” as used herein refers to a monocyclic aromatic 5-6 membered ring system containing one or more heteroatoms, for example one to three heteroatoms, such as nitrogen, oxygen, and sulfur. Where possible, said heteroaryl ring may be linked to the adjacent radical though carbon or nitrogen. Examples of heteroaryl rings include but are not limited to furan, thiophene, pyrrole, thiazole, oxazole, isothiazole, isoxazole, imidazole, pyrazole, triazole, pyridine or pyrimidine etc.

The terms “heterocyclyl” or “heterocyclic group” are art-recognized and refer to saturated or partially unsaturated 4- to 7-membered ring structures, whose ring structures include one to three heteroatoms, such as nitrogen, oxygen, and sulfur. Where possible, heterocyclyl rings may be linked to the adjacent radical through carbon or nitrogen. Examples of heterocyclyl groups include, but are not limited to, pyrrolidine, piperidine, morpholine, thiomorpholine, piperazine, oxetane, or azetidine.

The term “heterocyclyloxy” as used herein refers to a heterocyclyl group attached to oxygen (heterocyclyl-O—).

The term “heteroaryloxy” as used herein refers to a heteroaryl group attached to oxygen (heteroaryl-O—).

The terms “hydroxy” and “hydroxyl” as used herein refers to the radical —OH.

The term “oxo” as used herein refers to the radical ═O.

“Pharmaceutically or pharmacologically acceptable” include molecular entities and compositions that do not produce an adverse, allergic or other untoward reaction when administered to an animal, or a human, as appropriate. For human administration, preparations should meet sterility, pyrogenicity, general safety and purity standards as required by FDA Office of Biologics standards.

The term “pharmaceutically acceptable carrier” or “pharmaceutically acceptable excipient” as used herein refers to any and all solvents, dispersion media, coatings, isotonic and absorption delaying agents, and the like, that are compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. The compositions may also contain other active compounds providing supplemental, additional, or enhanced therapeutic functions.

The term “pharmaceutical composition” as used herein refers to a composition comprising at least one compound as disclosed herein formulated together with one or more pharmaceutically acceptable carriers.

“Individual,” “patient,” or “subject” are used interchangeably and include any animal, including mammals, preferably mice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep, horses, or primates, and most preferably humans. The compounds of the invention can be administered to a mammal, such as a human, but can also be administered to other mammals such as an animal in need of veterinary treatment, e.g., domestic animals (e.g., dogs, cats, and the like), farm animals (e.g., cows, sheep, pigs, horses, and the like) and laboratory animals (e.g., rats, mice, guinea pigs, and the like). The mammal treated in the methods of the invention is desirably a mammal in which treatment of obesity or weight loss is desired. “Modulation” includes antagonism (e.g., inhibition), agonism, partial antagonism and/or partial agonism.

In the present specification, the term “therapeutically effective amount” means the amount of the subject compound that will elicit the biological or medical response of a tissue, system or animal, (e.g. mammal or human) that is being sought by the researcher, veterinarian, medical doctor or other clinician. The compounds of the invention are administered in therapeutically effective amounts to treat a disease. Alternatively, a therapeutically effective amount of a compound is the quantity required to achieve a desired therapeutic and/or prophylactic effect, such as an amount which results in weight loss.

The term “pharmaceutically acceptable salt(s)” as used herein refers to salts of acidic or basic groups that may be present in compounds used in the compositions. Compounds included in the present compositions that are basic in nature are capable of forming a wide variety of salts with various inorganic and organic acids. The acids that may be used to prepare pharmaceutically acceptable acid addition salts of such basic compounds are those that form non-toxic acid addition salts, i.e., salts containing pharmacologically acceptable anions, including, but not limited to, malate, oxalate, chloride, bromide, iodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, salicylate, citrate, tartrate, oleate, tannate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate and pamoate (i.e., 1,1′-methylene-bis-(2-hydroxy-3-naphthoate)) salts. Compounds included in the present compositions that are acidic in nature are capable of forming base salts with various pharmacologically acceptable cations. Examples of such salts include alkali metal or alkaline earth metal salts and, particularly, calcium, magnesium, sodium, lithium, zinc, potassium, and iron salts. Compounds included in the present compositions that include a basic or acidic moiety may also form pharmaceutically acceptable salts with various amino acids. The compounds of the disclosure may contain both acidic and basic groups; for example, one amino and one carboxylic acid group. In such a case, the compound can exist as an acid addition salt, a zwitterion, or a base salt.

The compounds of the disclosure may contain one or more chiral centers and, therefore, exist as stereoisomers. The term “stereoisomers” when used herein consist of all enantiomers or diastereomers. These compounds may be designated by the symbols “(+),” “(−).” “R” or “S,” depending on the configuration of substituents around the stereogenic carbon atom, but the skilled artisan will recognize that a structure may denote a chiral center implicitly. The present invention encompasses various stereoisomers of these compounds and mixtures thereof. Mixtures of enantiomers or diastereomers may be designated “(±)” in nomenclature, but the skilled artisan will recognize that a structure may denote a chiral center implicitly.

The compounds of the disclosure may contain one or more double bonds and, therefore, exist as geometric isomers resulting from the arrangement of substituents around a carbon-carbon double bond. The symbol

denotes a bond that may be a single, double or triple bond as described herein. Substituents around a carbon-carbon double bond are designated as being in the “Z” or “E” configuration wherein the terms “Z” and “E” are used in accordance with IUPAC standards. Unless otherwise specified, structures depicting double bonds encompass both the “E” and “Z” isomers. Substituents around a carbon-carbon double bond alternatively can be referred to as “cis” or “trans,” where “cis” represents substituents on the same side of the double bond and “trans” represents substituents on opposite sides of the double bond. Mixtures of compounds with substituents disposed on both the same and opposite sides of the double bond are designated “cis/trans.”

Compounds of the disclosure may contain a carbocyclic or heterocyclic ring and therefore, exist as geometric isomers resulting from the arrangement of substituents around the ring. The arrangement of substituents around a carbocyclic or heterocyclic ring are designated as being in the “Z” or “E” configuration wherein the terms “Z” and “E” are used in accordance with IUPAC standards. Unless otherwise specified, structures depicting carbocyclic or heterocyclic rings encompass both “Z” and “E” isomers. Substituents around a carbocyclic or heterocyclic rings may also be referred to as “cis” or “trans”, where the term “cis” represents substituents on the same side of the plane of the ring and the term “trans” represents substituents on opposite sides of the plane of the ring. Mixtures of compounds wherein the substituents are disposed on both the same and opposite sides of plane of the ring are designated “cis/trans.”

Individual enantiomers and diasteriomers of compounds of the present invention can be prepared synthetically from commercially available starting materials that contain asymmetric or stereogenic centers, or by preparation of racemic mixtures followed by resolution methods well known to those of ordinary skill in the art. These methods of resolution are exemplified by (1) attachment of a mixture of enantiomers to a chiral auxiliary, separation of the resulting mixture of diastereomers by recrystallization or chromatography and liberation of the optically pure product from the auxiliary, (2) salt formation employing an optically active resolving agent, (3) direct separation of the mixture of optical enantiomers on chiral liquid chromatographic columns or (4) kinetic resolution using stereoselective chemical or enzymatic reagents. Racemic mixtures can also be resolved into their component enantiomers by well known methods, such as chiral-phase liquid chromatography or crystallizing the compound in a chiral solvent. Stereo selective syntheses, a chemical or enzymatic reaction in which a single reactant forms an unequal mixture of stereoisomers during the creation of a new stereocenter or during the transformation of a pre-existing one, are well known in the art. Stereoselective syntheses encompass both enantio- and diastereoselective transformations, and may involve the use of chiral auxiliaries. For examples, see Carrcira and Kvaerno, Classics in Stereoselective Synthesis, Wiley-VCII: Weinheim, 2009.

The compounds disclosed herein can exist in solvated as well as unsolvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like, and it is intended that the invention embrace both solvated and unsolvated forms. In one embodiment, the compound is amorphous. In one embodiment, the compound is a single polymorph. In another embodiment, the compound is a mixture of polymorphs. In another embodiment, the compound is in a crystalline form.

The invention also embraces isotopically labeled compounds of the invention which are identical to those recited herein, except that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine and chlorine, such as ²H, ³H, ¹³C, ¹⁴C, ¹⁵N, ¹⁸O, ¹⁷O, ³¹P, ³²P, ³⁵S, ¹⁸F, and ³⁶Cl, respectively. For example, a compound of the invention may have one or more H atom replaced with deuterium.

Certain isotopically-labeled disclosed compounds (e.g., those labeled with ³H and ¹⁴C) are useful in compound and/or substrate tissue distribution assays. Tritiated (i.e., ³H) and carbon-14 (i.e., ¹⁴C) isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with heavier isotopes such as deuterium (i.e., ²H) may afford certain therapeutic advantages resulting from greater metabolic stability (e.g., increased in vivo half-life or reduced dosage requirements) and hence may be preferred in some circumstances. Isotopically labeled compounds of the invention can generally be prepared by following procedures analogous to those disclosed in the examples herein by substituting an isotopically labeled reagent for a non-isotopically labeled reagent.

The term “prodrug” refers to compounds that are transformed in vivo to yield a disclosed compound or a pharmaceutically acceptable salt, hydrate or solvate of the compound. The transformation may occur by various mechanisms (such as by esterase, amidase, phosphatase, oxidative and or reductive metabolism) in various locations (such as in the intestinal lumen or upon transit of the intestine, blood or liver). Prodrugs are well known in the art (for example, see Rautio, Kumpulainen, et al, Nature Reviews Drug Discovery 2008, 7, 255). For example, if a compound of the invention or a pharmaceutically acceptable salt, hydrate or solvate of the compound contains a carboxylic acid functional group, a prodrug can comprise an ester formed by the replacement of the hydrogen atom of the acid group with a group such as (C₁₋₈)alkyl, (C₂₋₁₂)alkanoyloxymethyl, 1-(alkanoyloxy)ethyl having from 4 to 9 carbon atoms, 1-methyl-1-(alkanoyloxy)-ethyl having from 5 to 10 carbon atoms, alkoxycarbonyloxymethyl having from 3 to 6 carbon atoms, 1-(alkoxycarbonyloxy)ethyl having from 4 to 7 carbon atoms, 1-methyl-1-(alkoxycarbonyloxy)ethyl having from 5 to 8 carbon atoms, N-(alkoxycarbonyl)aminomethyl having from 3 to 9 carbon atoms, 1-(N-(alkoxycarbonyl)amino)ethyl having from 4 to 10 carbon atoms, 3-phthalidyl, 4-crotonolactonyl, gamma-butyrolacton-4-yl, di-N,N-(C₁₋₂)alkylamino(C₂₋₃)alkyl (such as β-dimethylaminoethyl), carbamoyl-(C₁₋₂)alkyl, N,N-di(C₁₋₂)alkylcarbamoyl-(C₁₋₂)alkyl and piperidino-, pyrrolidino- or morpholino (C₂₋₃)alkyl.

Similarly, if a compound of the invention contains an alcohol functional group, a prodrug can be formed by the replacement of the hydrogen atom of the alcohol group with a group such as (C₁₋₆)alkanoyloxymethyl, 1-((C₁₋₆)alkanoyloxy)ethyl, 1-methyl-1-((C₁₋₆)alkanoyloxy)ethyl (C₁₋₆)alkoxycarbonyloxymethyl, N-(C₁₋₆)alkoxycarbonylaminomethyl, succinoyl, (C₁₋₆)alkanoyl, α-amino(C₁₋₄)alkanoyl, arylacyl and α-aminoacyl, or α-aminoacyl-α-aminoacyl, where each α-aminoacyl group is independently selected from the naturally occurring L-amino acids, P(O)(OH)₂, —P(O)(O(C₁₋₆)alkyl)₂ or glycosyl (the radical resulting from the removal of a hydroxyl group of the hemiacetal form of a carbohydrate).

If a compound of the invention incorporates an amine functional group, a prodrug can be formed, for example, by creation of an amide or carbamate, an N-acyloxyakyl derivative, an (oxodioxolenyl)methyl derivative, an N-Mannich base, imine or enamine. In addition, a secondary amine can be metabolically cleaved to generate a bioactive primary amine, or a tertiary amine can metabolically cleaved to generate a bioactive primary or secondary amine. For examples, see Simplicio, et al., Molecules 2008, 13, 519 and references therein.

I. Tricyclic Compounds

In certain embodiments, the present invention provides compounds of formula I:

wherein

B is a 5-membered heteroaryl having one or two heteroatoms independently selected from the group consisting of S, O or N, optionally substituted on a carbon with one, or two substituents each independently selected from R^(B1), and, optionally substituted, on nitrogen, if present, with one or two substituents each independently selected from R^(B2);

D is a 6- or 7-membered heterocyclic, carbocyclic, heteroaryl or aryl ring; wherein B is fused to D such that the two atoms shared by D and B are both carbon;

E is selected from the group consisting of: —W—C(R^(C3)R^(C4))—; —W—C(═O)—; —C(═O)—V—; —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—; —C(R^(C1)R^(C2))—V—; —N═C(R^(D2))—; —C(R^(D1))═N—; —C(R^(D1))═C(R^(D2))—; —N═N—; —W—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—V—C(═O)—; —W—C(═O)—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—C(═O)—U—; —C(═O)—V—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—U—; —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—; and —C(R^(C1)R^(C2))—V—C(R^(C5)R^(C6))—; wherein the left hand substituent of E is attached to the phenyl ring of Formula I and the right hand substituent of E is attached to B;

W is selected from the group consisting of O, S, and N(R^(N1));

V is selected from the group consisting of O, S, and N(R^(N2));

U is selected from the group consisting of O, S, and N(R^(N3));

Y is: —C(R^(Y1)R^(Y2))— or —N(R^(Y3))—;

X is selected from the group consisting of —S—, —S(═O)—, —SO₂— with the proviso that, if Y is —N(R^(Y3))—, then X is —SO₂—;

A is a ring selected from the group consisting of phenyl, a 5-6 membered heteroaryl having 1, 2 or 3 heteroatoms each selected from S, N or O, and a 4-7 membered heterocycle having 1, 2 or 3 heteroatoms each selected from N or O;

R^(A1) is selected, independently for each occurrence, from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl or C₁₋₃alkoxy, wherein C₁₋₄alkyl, or C₁₋₃alkoxy may be optionally substituted by one or more halogens;

n is 1 or 2;

R^(A2) is selected from the group consisting of hydrogen, R^(i)R^(j)N—, heterocyclyl, heterocyclyloxy, heterocyclyl-(NR^(a))—; wherein said heterocyclyl is a 4-7 membered ring optionally substituted by one or more substituents selected from R^(g) and wherein if said heterocyclyl contains a —NH moiety that nitrogen may be optionally substituted by one or more groups R^(h); or

R^(A2) is selected from the group consisting of C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1 or 2), C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl, C₁₋₆alkyl-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—, C₁₋₆alkoxy-carbonyl-N(R^(a))—, C₁₋₆alkyl-carbonyl-N(R^(a))—C₁₋₆alkyl, C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl, C₁₋₆alkoxyC₁₋₆alkyl; wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)—, C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-, C₁₋₆alkyl-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—, C₁₋₆alkoxycarbonyl-N(R^(a))—, C₁₋₆alkyl-carbonyl-N(R^(a))C₁₋₆alkyl-, C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl-, C₁₋₆alkoxy-C₁₋₆alkyl may be optionally substituted by R^(P2), phenyl, phenoxy, heteroaryl, heteroaryloxy, heteroaryl-(NR^(a))—, heterocyclyl, heterocyclyloxy or heterocyclyl-N(R^(a))—; wherein said heteroaryl is a 5-6 membered monocyclic ring having one, two or three heteroatoms selected from O, S, or N, and wherein said heteroaryl or phenyl is optionally substituted with one or more substituents selected from R^(f); wherein said heterocyclyl is a 4-7 membered ring optionally substituted by one or more substituents selected from R^(g) and wherein if said heterocyclyl contains a —NH moiety that nitrogen may be optionally substituted by one or more groups R^(h);

R^(B1) is selected, independently for each occurrence, from the group consisting of hydrogen, cyano, halogen, C₁₋₂alkyl or C₁₋₂alkoxy, wherein C₁₋₂alkyl or C₁₋₂alkoxy, may be optionally substituted with one or more halogens;

R^(B2) is selected, independently for each occurrence, from the group consisting of hydrogen or C₁₋₂alkyl, wherein C₁₋₂alkyl may be optionally substituted with one or more halogens;

R^(Y1) and R^(Y2) are independently selected from the group consisting of hydrogen, C₁₋₄alkyl;

R^(Y3) is selected from the group consisting of hydrogen, C₁₋₄alkyl;

R^(C1) and R^(C2) are each selected independently from the group consisting of hydrogen, halogen, hydroxyl, C₁₋₂alkyl, C₁₋₂alkoxy, wherein C₁₋₂alkyl or C₁₋₂alkoxy may be optionally substituted by one or more substituents selected from halogen, cyano or hydroxyl;

R^(N1) is selected from the group consisting of hydrogen and C₁₋₂alkyl, wherein C₁₋₂alkyl may be optionally substituted by one or more substituents selected from halogen, cyano or hydroxyl;

R^(D1) is selected from the group consisting of hydrogen, halogen, C₁₋₂alkyl, C₁₋₂alkoxy; and wherein C₁₋₂alkyl, and C₁₋₂alkoxy may be optionally substituted by halogen, cyano or hydroxyl;

R^(C3) and R^(C4) are selected independently from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy and wherein C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy may be optionally substituted by one or more substituents selected from R^(P1);

R^(N2) is selected for each occurrence from the group consisting of hydrogen, C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl or C₃₋₄alkynyl, and wherein C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl, or C₃₋₄alkynyl may be optionally substituted by one or more substituents selected from R^(P1);

R^(D2) is selected from the group consisting of hydrogen, halogen, cyano, hydroxyl, C₁₋₄alkyl, C₁₋₃alkoxy, C₂₋₄alkynyl, C₂₋₄alkenyl, C₁₋₃alkyl-carbonyl-N(R^(a))— and wherein C₁₋₄alkyl, C₁₋₃alkoxy, C₂₋₄alkynyl, C₂₋₄alkenyl and C₁₋₃alkyl-carbonyl-N(R^(a))— may be optionally substituted by one or more substituents selected from R^(P1);

R^(C5) and R^(C6) are selected independently from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy and wherein C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy may be optionally substituted by one or more substituents selected from R^(P1);

R^(N3) is selected for each occurrence from the group consisting of hydrogen, C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl or C₃₋₄alkynyl, and wherein C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl, or C₃₋₄alkynyl may be optionally substituted by one or more substituents selected from R^(P1);

R^(a) and R^(b) are independently selected, for each occurrence, from the group consisting of hydrogen and C₁₋₄alkyl, or R^(a) and R^(b), together with the nitrogen to which they are attached, may form a 4-6 membered heterocyclic ring which may have an additional heteroatom selected from O, S, or N, and wherein C₁₋₄alkyl may be optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, oxo and hydroxyl, and wherein the 4-6 membered heterocyclic ring may be optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, oxo or hydroxyl;

R^(f) is independently selected, for each occurrence, from the group consisting of R^(P2), hydrogen, halogen, cyano, hydroxyl, C₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1 or 2), C₁₋₆alkylcarbonyl-N(R^(a))—; C₁₋₆alkoxycarbonyl-N(R^(a))—; and wherein C₁₋₆alkyl, C₃₋₆cycloalkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆-cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, C₁₋₆alkylcarbonyl-N(R^(a))—, C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one or more substituents selected from R^(P2);

R^(g) is independently selected for each occurrence from the group consisting of R^(P2) hydrogen, halogen, cyano, hydroxyl, oxo, C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1 or 2), C₁₋₆alkylcarbonyl-N(R^(a))—; C₁₋₆alkoxycarbonyl-N(R^(a))—, and wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, C₁₋₆alkylcarbonyl-N(R^(a))—; C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one or more substituents selected from R^(P2);

R^(h) is independently selected for each occurrence from the group consisting of R^(P3), hydrogen, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—, C₁₋₆alkoxycarbonyl-; and wherein C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—, C₁₋₆alkylcarbonyl- may be optionally substituted by one or more substituents selected from R^(P2);

R^(i) and R^(j), are selected independently for each occurrence from group consisting of hydrogen, C₁₋₄alkyl and C₃₋₆cycloalkyl optionally substituted by one or more substituents selected from R^(P1); or R^(i) and R^(j) taken together with the nitrogen to which they are attached form a 4-7 membered heterocyclyl ring which may have an additional heteroatom selected from O, S, or N, optionally substituted on carbon by one or more substituents selected from the group consisting of halogen, hydroxyl, oxo, cyano, C₁₋₆alkyl, C₁₋₆alkoxy, R^(a)R^(b)N—, R^(a)R^(b)N—SO₂—, R^(a)R^(b)N-carbonyl-, and wherein C₁₋₆alkyl or C₁₋₆alkoxy may be optionally substituted by R^(P4); or optionally substituted on nitrogen by one or more substituents selected from the group consisting of C₁₋₆alkyl, R^(a)R^(b)N-carbonyl-, and wherein C₁₋₆alkyl may be optionally substituted by R^(P4);

R^(P1) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano, R^(a)R^(b)N—, R^(a)R^(b)N-carbonyl-, C₁₋₃alkoxy;

R^(P2) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano, C₁₋₆alkoxy, R^(i)R^(j)N—, R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂—, R^(i)R^(j)N-carbonyl-N(R^(a))—;

R^(P3) is independently selected, for each occurrence, from the group consisting of, R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂—;

R^(P4) is independently selected, for each occurrence, from the group consisting of, halogen, hydroxyl, cyano; and

pharmaceutically acceptable salts, stereoisomers, esters and prodrugs thereof.

For example, ring B may, in certain embodiments, be selected from the group consisting of:

wherein the * and the ⁺ indicate the points of attachment to ring D as indicated in Structure A:

Exemplary B rings that may form part of the contemplated tricyclic core may include those selected from the group consisting of:

For example, B may be the ring:

In certain embodiments E may have moiety as above, wherein for example, W is O or NR^(N1), V is O or NR^(N2) and/or U may be O or NR^(N3). For example, E is selected from the group consisting of: —O—C(R^(C3)R^(C4))—; —O—C(═O)—; —N(R^(N1))—C(═O)—; —N(R^(N1))—C(═O)—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—O—; —N═C(R^(D2))—; —C(R^(D1))═N—; —C(R^(D1))═C(R^(D2))—; —N═N—; —O—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—O—C(═O)—; —O—C(═O)—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—C(═O)—N(R^(N3))—; —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—O—; —C(R^(C1)R^(C2))—N(R^(N2))—C(═O)—; and —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—. In another embodiment, R^(C3), R^(C4). R^(C5), R^(C6), and R^(D2) that form part of E may be selected from the group consisting of: hydrogen, hydroxyl, C₁₋₄alkyl and fluorine. In an embodiment, R^(N2) and R^(N3) that form part of E may be selected from the group consisting of hydrogen and C₁₋₄-alkyl. In another embodiment, R^(C1), R^(C2), R^(D1), and R^(N1) that form part of E may be selected from hydrogen or C₁₋₂ alkyl. Exemplary E moities may be selected from the group consisting of, for example, —O—CH₂—; —O—CH(CH₃)—; —O—C(═O)—; —N(R^(N1))—C(═O); —O—CH₂CH₂—; —N═CH—; and —CH═N—.

Provided herein, for example, are tricyclic compounds represented by formulas IIa, IIb, and IIc:

wherein R^(C3), R^(C4), R^(C5) and R^(C6) are, independently for each occurrence, selected from the group consisting of: hydrogen, fluorine, and C₁₋₄alkyl, wherein C₁₋₄alkyl may be optionally substituted by one or more substituents selected from the group consisting of halogen, hydroxyl, cyano, or NH₂. A, R^(A2), and R^(A1) and n may be as described above for formula I, for example, n may be 1, and R^(A1) may be hydrogen or halogen.

In certain embodiments, the Y moiety of a provided formula may be —N(R^(Y3))—, and/or X may be —SO₂—. In other embodiments, A may be phenyl, R^(A1) may be hydrogen or halogen, and R^(A2) may be selected from the group consisting of hydrogen, halogen, C₁₋₆alkyl or C₃₋₆alkenyl, (wherein the C₁₋₆alkyl or the C₃₋₆alkenyl may be optionally substituted by R^(i)R^(j)N—, as defined above) and n may be 1 or 2. For example, A may be phenyl, R^(A1) may be hydrogen or fluorine, and R^(A2) may be hydrogen, C₁₋₆alkyl or C₃₋₆alkenyl, wherein the C₁₋₆alkyl or C₃₋₆alkenyl may be optionally substituted by R^(i)R^(j)N—, e.g. (C₁₋₄alkyl)(C₁₋₄alkyl)N—.

Also provided herein is a compound represented by formula III:

wherein:

E is selected from the group consisting of: —O—C(R^(C3)R^(C4))—; —O—C(═O)—; —N(R^(N1))—C(═O)—; —N(R^(N1))—C(═O)—C(R^(C5)R^(C6))—; C(R^(C1)R^(C2))—O—; —N═C(R^(D2))—; —C(R^(D1))═N—; —C(R^(D1))═C(R^(D2))—; —N═N—; —O—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—O—C(═O)—; —O—C(═O)—C(R^(C5)R^(C6))—; —C(R^(C1)R^(C2))—C(═O)—N(R^(N3))—; —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—O—; —C(R^(C1)R^(C2))—N(R^(N2))—C(═O)—; and —C(R^(C1)R^(C2))—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—;

Y is: —C(R^(Y1)R^(Y2))— or —N(R^(Y3))—;

R^(A1) is selected from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl or C₁₋₃alkoxy, wherein C₁₋₄alkyl, or C₁₋₃alkoxy may be optionally substituted by one or more halogens;

R^(A2) is selected from the group consisting of hydrogen, R^(i)R^(j)N—, heterocyclyl, heterocyclyloxy, heterocyclyl-(NR^(a))—; wherein said heterocyclyl is a 4-7 membered ring optionally substituted by one or more substituents selected from R^(g) and wherein if said heterocyclyl contains a —NH moiety that nitrogen may be optionally substituted by one or more groups R^(h); or

R^(A2) is selected from the group consisting of C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1 or 2), C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl, C₁₋₆alkyl-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—, C₁₋₆alkoxy-carbonyl-N(R^(a))—, C₁₋₆alkyl-carbonyl-N(R^(a))C₁₋₆alkyl, C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl, C₁₋₆alkoxy-C₁₋₆alkyl; wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, C₃₋₆cycloalkoxy, C₁₋₆alkyl-S(O)₂—, C₁₋₆alkyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl, C₁₋₆alkyl-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))-carbonyl-N(R^(a))—, C₁₋₆alkyl-N(R^(a))—SO₂—, C₁₋₆alkyl-SO₂—N(R^(a))—, C₁₋₆alkoxycarbonyl-N(R^(a))—, C₁₋₆alkyl-carbonyl-N(R^(a))C₁₋₆alkyl, C₁₋₆alkyl-N(R^(a))-carbonyl-C₁₋₆alkyl-, C₁₋₆alkoxyC₁₋₆alkyl may be optionally substituted by R^(P2), heterocyclyl, heterocyclyloxy or heterocyclyl-N(R^(a))—; and wherein if said heterocyclyl contains a —NH moiety that nitrogen may be optionally substituted by one or more groups R^(h);

R^(Y1) and R^(Y2) are independently selected from the group consisting of hydrogen and C₁₋₄alkyl;

R^(Y3) is selected from the group consisting of hydrogen and C₁₋₄alkyl;

R^(C1) and R^(C2) are each selected independently from the group consisting of hydrogen, halogen, hydroxyl, C₁₋₂alkyl, C₁₋₂alkoxy, wherein C₁₋₂alkyl or C₁₋₂alkoxy may be optionally substituted by one or more substituents selected from halogen, cyano or hydroxyl;

R^(N1) is selected from the group consisting of hydrogen and C₁₋₂alkyl, wherein C₁₋₂alkyl may be optionally substituted by one or more substituents selected from halogen, cyano or hydroxyl

R^(D1) is selected from the group consisting of hydrogen, halogen, C₁₋₂alkyl, C₁₋₂alkoxy; and wherein C₁₋₂alkyl, and C₁₋₂alkoxy may be optionally substituted by halogen, cyano or hydroxyl;

R^(C3) and R^(C4) are selected independently from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy and wherein C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy may be optionally substituted by one or more substituents selected from R^(P1);

R^(N2) is selected for each occurrence from the group consisting of hydrogen, C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl or C₃₋₄alkynyl, and wherein C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl, or C₃₋₄alkynyl may be optionally substituted by one or more substituents selected from R^(P1);

R^(D2) is selected from the group consisting of hydrogen, halogen, cyano, hydroxyl, C₁₋₄alkyl, C₁₋₃alkoxy, C₂₋₄alkynyl, C₂₋₄alkenyl, C₁₋₃alkyl-carbonyl-N(R^(a))— and wherein C₁₋₄alkyl, C₁₋₃alkoxy, C₂₋₄alkynyl, C₂₋₄alkenyl and C₁₋₃alkyl-carbonyl-N(R^(a))— may be optionally substituted by one or more substituents selected from R^(P1);

R^(C5) and R^(C6) are selected independently from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy and wherein C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy may be optionally substituted by one or more substituents selected from R^(P1);

R^(N3) is selected for each occurrence from the group consisting of hydrogen, C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄alkenyl or C₃₋₄alkynyl, and wherein C₁₋₄alkyl, C₁₋₃alkylcarbonyl, C₃₋₄-alkenyl, or C₃₋₄alkynyl may be optionally substituted by one or more substituents selected from R^(P1);

R^(a) and R^(b) are independently selected, for each occurrence, from the group consisting of hydrogen and C₁₋₄alkyl, or R^(a) and R^(b), together with the nitrogen to which they are attached, may form a 4-6 membered heterocyclic ring which may have an additional heteroatom selected from O, S, or N, and wherein C₁₋₄alkyl may be optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, oxo and hydroxyl, and wherein the 4-6 membered heterocyclic ring may be optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, oxo or hydroxyl;

R^(g) is independently selected for each occurrence from the group consisting of R^(P2), hydrogen, halogen, cyano, hydroxyl, oxo, C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)— (wherein w is 0, 1 or 2), C₁₋₆alkylcarbonyl-N(R^(a))—; C₁₋₆alkoxycarbonyl-N(R^(a))—, and wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₁₋₆alkyl-S(O)_(w)—, C₁₋₆alkylcarbonyl-N(R^(a))—; C₁₋₆alkoxycarbonyl-N(R^(a))— may be optionally substituted by one or more substituents selected from R^(P2);

R^(h) is independently selected for each occurrence from the group consisting of R^(P3), hydrogen, C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—; C₁₋₆alkoxycarbonyl-; and wherein C₁₋₆alkyl, C₃₋₆alkenyl, C₃₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkyl-S(O)₂—, C₁₋₆alkylcarbonyl- may be optionally substituted by one or more substituents selected from R^(P2);

R^(i) and R^(j), are selected independently for each occurrence from group consisting of hydrogen, C₁₋₄alkyl and C₃₋₆cycloalkyl optionally substituted by one or more substituents selected from R^(P1); or R^(i) and R^(j) taken together with the nitrogen to which they are attached form a 4-7 membered heterocyclyl ring which may have an additional heteroatom selected from O, S, or N, optionally substituted on carbon by one or more substituents selected from the group consisting of halogen, hydroxyl, oxo, cyano, C₁₋₆alkyl, C₁₋₆alkoxy,R^(a)R^(b)N—, R^(a)R^(b)N—SO₂—, R^(a)R^(b)N-carbonyl-, and wherein C₁₋₆alkyl or C₁₋₆alkoxy may be optionally substituted by R^(P4); or optionally substituted on nitrogen by one or more substituents selected from the group consisting of C₁₋₆alkyl, R^(a)R^(b)N-carbonyl-, and wherein C₁₋₆alkyl may be optionally substituted by R^(P4);

R^(P1) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano, R^(a)R^(b)N—, R^(a)R^(b)N-carbonyl-, C₁₋₃alkoxy;

R^(P2) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano, C₁₋₆alkoxy, R^(i)R^(j)N—, R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂—, R^(i)R^(j)N-carbonyl-N(R^(a))—;

R^(P3) is independently selected, for each occurrence, from the group consisting of R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂—;

R^(P4) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano; and pharmaceutically acceptable salts, stereoisomers, esters and prodrugs thereof.

Also provided herein are compounds that may be selected from the group consisting of: 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylic acid; 8-(benzenesulfonylmethyl)-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid; 7-(benzenesulfonylmethyl)-furo[2,3-c]quinoline-6-carboxylic acid; 7-(benzenesulfonyl-methyl)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-(benzenesulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 8-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluoro-benzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid; 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylic acid; 8-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylamino-prop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-(R)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-methyl]-(S)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-(3-diethylaminopropyl)-4-fluoro-benzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-chromeno[3,4-d]iso-thiazole-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-benzenesulfonylamino-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]-chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4,5-dihydrofuro[2,3-c]-quinoline-6-carboxylic acid; 7-{2-[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-(3-hydroxyazetidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((E)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylic acid or pharmaceutically acceptable salts, stereoisomers, esters and prodrugs thereof.

Procedures for making compounds described herein are provided below with reference to Schemes 1-4. In the reactions described below, it may be necessary to protect reactive functional groups (such as hydroxy, amino, thio or carboxy groups) to avoid their unwanted participation in the reactions. The incorporation of such groups, and the methods required to introduce and remove them are known to those skilled in the art (for example, see Greene, Wuts, Protective Groups in Organic Synthesis. 2nd Ed. (1999)). The deprotection step may be the final step in the synthesis such that the removal of protecting groups affords compounds of Formula I, as disclosed herein, or as exemplified in, for example, General Formula I, below. Starting materials used in the following schemes can be purchased or prepared by methods described in the chemical literature, or by adaptations thereof, using methods known by those skilled in the art. The order in which the steps are performed can vary depending on the groups introduced and the reagents used, but would be apparent to those skilled in the art.

The general synthetic strategy used to prepare the tricyclic compounds of General Formula I is depicted in Scheme 1. The tricyclic system may be assembled in a variety of ways, starting from an appropriately substituted and protected phenyl ring 1A. The group F′ is a suitably protected carboxylic acid, such as a methyl- or t-butyl carboxylate or is a functional group that may be readily converted into a carboxylic acid, such as a nitrile or aldehyde. The group F is a thioether, sulfoxide, sulfone or sulfonamide group, or a functional group that may be subsequently converted into a thioether, sulfoxide, sulfone or sulfonamide group. The B-ring can be directly attached to the substituted phenyl ring 1A, to give intermediate 1B, and then the D-ring can be formed by an intra-molecular reaction to give intermediate 1E. Alternatively, the B-ring can be attached to the substituted phenyl ring 1A via a linker, E, to give intermediate 1C, and then the D-ring can be formed by an intra-molecular reaction to give intermediate 1E. Alternatively, the D-ring can be built up onto the substituted phenyl ring to give intermediate 1D, and then the B-ring assembled to give intermediate 1E. Compounds of Formula I can be prepared from intermediate 1E by removal of any protecting groups. Alternatively, further modifications may be made to 1E, such as modifications at F, before the removal of any protecting groups to give compounds of Formula I. Specific steps in the synthetic process are described in more detail below.

[Scheme 1, Step 1(i)] Compounds of structure 1A may be coupled under a range of conditions to compounds of structure 1B′, where B is a five-membered heterocyclic ring to afford compounds of the type 1B. The introduction of the B ring may require a number of steps and the preparation of a number of intermediates. Protecting groups may also be required. If R¹ is a suitable functional group (such as a halide or triflate), 1B′ can be introduced by the formation of a carbon-carbon bond to afford 1B. The carbon-carbon bond can be formed by reacting compounds of structure 1B′ where R³ is a borane, boronate or boronic acid group (such as a 2-formylfuran-3-boronate) in the presence of a palladium catalyst (such as palladium chloride dppf adduct or tris-(dibenzylideneacetone)-dipalladium), in the presence of a base (such as cesium carbonate) and a suitable reagent (such as a phosphine, for example, tri-tert-butyl-phosphonium tetrafluoroborate or triphenylphosphine) in an appropriate solvent (such as dichloromethane, dioxane, water or tetrahydrofuran, or mixtures thereof) and under appropriate conditions (such as heating, for example heating at 80-120° C. for 1-2 hours or microwave irradiation at 120-160° C. for 10 minutes to 1 hour) to afford 1B. A wide range of appropriate reagents and conditions are known to those skilled in the art to couple organoboranes, boronates and boronic acids to 1A. [For example, see Miyaura, Suzuki, Chem. Rev. 1995, 95, 2457; Suzuki, Modern Arene Chemistry (2002), 53-106].

[Scheme 1, Step 1(i)] Alternatively the carbon-carbon bond can be formed by using compounds of structure 1B′ where R³ is a substituted trialkylstannane (such as a heterocyclic tri-n-butylstannane) in the presence of a palladium catalyst (such as palladium chloride dppf adduct with DCM), in an appropriate solvent (such as dimethoxyethane or tetrahydrofuran) and under appropriate conditions (such as heating, at 80-120° C. for 1-2 hours or by microwave irradiation at 120-160° C. for 10 minutes to 1 hour) to afford 1B. A wide range of appropriate reagents and conditions are known to those skilled in the art to couple heteroaryl stannanes to aryl halides such as 1A. [For example, see Smith, March, March's Advanced Organic Chemistry, 5^(th) Edition, Wiley: New York, 2001, pp. 931-932; De Souza, Current Organic Synthesis (2006), 3(3), 313-326].

[Scheme 1, Step 1(i)] Alternatively compounds of structure 1A, where R¹ is a suitable group (such as a halide or triflate), can be treated with a diboronate (such as bis-pinacolatodiboron) in the presence of a palladium catalyst (such as palladium chloride dppf adduct) and a base (such as potassium acetate or diisopropylamine) in an appropriate solvent (such as dioxane/water) and under appropriate conditions (such as heating for example at 80-120° C. for 1-2 hours or by microwave irradiation at 120-160° C. for 10 minutes to 1 hour) to give a compound of structure 1A, where R¹ is a boronate. A wide range of appropriate reagents and conditions are known to those skilled in the art to convert an arylhalide (or aryl triflate) to an arylboronate (or an arylborane) [for example, see Marshall Chemtracts (2000), 13(4), 219-222]. The arylborane (or arylboronate) thus formed, can then be treated with compounds of structure 1B′ (where R³ is a halogen or triflate) in the presence of suitable reagents such as a phosphine (such as tri-tert-butyl-phosphonium tetrafluoroborate), a base (such as cesium carbonate) and a catalyst (such as tris-(dibenzylideneacetone)-dipalladium) in an appropriate solvent (such as water/dioxane) under appropriate conditions (such as heating at 80-120° C. for 1-2 hours or by microwave irradiation at 120-160° C. for 10 minutes to 1 hour) to afford compounds of the structure 1B.

[Scheme 1, Step 1(iv)] The groups R² and R⁴ of compound 1B can be coupled together to give the group E, which forms the D-ring. R² or R⁴ may have been masked by protecting groups during Step 1(i), and may require deprotection before the group E can be formed. Alternatively, R² or R⁴ may require chemical modification before the group E can be formed. For example if R² or R⁴ is a nitro group, that group may be treated with a reducing agent (such as hydrogen in the presence of a suitable catalyst, such as palladium on carbon; or treated with an inorganic reducing agent such as tin (II) chloride in DMF) to give an amino group. For example, if R² or R⁴ is a hydroxyalkyl group, that group may be treated with an oxidising agent (such as the Jones reagent or manganese dioxide) to give an aldehyde or with a different oxidising agent (such as potassium permanganate) to give a carboxylic acid. For example, if R² or R⁴ is an aldehyde, that group may be treated with an oxidising agent (such as potassium permanganate) to give a carboxylic acid or with a reducing agent (such as sodium borohydride) to give an alcohol. For example, if R² or R⁴ is a ketone, that group may be treated with a reducing agent (such as sodium borohydride) to give a secondary alcohol. For example, if R² or R⁴ is a carboxylic acid or ester, that group may be treated with a reducing agent (such as lithium aluminium hydride) to give an alcohol. For example, if R² or R⁴ is an alkene group, that group may be treated with a borane (such as 9-borobicyclononane) and converted to a primary or secondary alcohol.

[Scheme 1, Step 1(iv)] For example, if one of the two groups R² or R⁴ is a hydroxyl and the other group is a substituted alkylalcohol then 1B can be treated with a dehydrating agent (such as diisopropyl azodicarboxylate in the presence of a phosphine, such as triphenylphosphine) to give 1E, where E is an ether. Alternatively, if one of the two groups R² or R⁴ is a hydroxyl and the other group is an alkyl group substituted with a leaving group (such as a halogen, or a triflate) 1B can be treated with a base (such as diisopropylethylamine, potassium carbonate or sodium hydride) to form 1E, where E is an ether.

Alternatively, if one of the groups R² or R⁴ is a carboxylic acid and the other group is an alkylhalide or sulfonate, then 1B can be treated with a base such as diisopropylethyl amine, potassium carbonate or sodium hydride to form 1E, where E is an ester.

Alternatively, if one of the two groups R² or R⁴ is a hydroxyl, or substituted alkylalcohol and the other group is a carboxylic acid or carboxylic ester, then 1B can be treated with an acid (such as hydrochloric acid) or dehydrating agent (such as dicyclohexylcarbodiimide or acetic anhydride) to form 1E, where E is an ester.

Alternatively, if one of the two groups R² or R⁴ on 1B is a hydroxyl or substituted alkylalcohol and the other group is a carboxylic acid, then the carboxylic acid can first be converted to a mixed anhydride (for example by treatment with 2,4,6-trichlorobenzoyl chloride) or to an active ester (for example by treatment with HATU in the presence of a base such as DIPEA or pyridine), and the resulting mixed anhydride or active ester can then be further treated with a base (such as diisopropylethylamine, pyridine or potassium carbonate) to form 1E, where E is an ester.

Alternatively, if one of the groups R² or R⁴ on 1B is an amine or a substituted alkylamine and the other group is a carboxylic acid, the carboxylic acid can be converted to an active ester (for example by treatment with HATU and a base such as diisopropylethylamine or pyridine or TBTU in the presence of N-methylmorpholine), and the resulting active ester can be further treated with a base to form 1E where E is an amide.

Alternatively, if one of the two groups R² or R⁴ on 1B is an amine, or a substituted alkylamine and the other group is a carboxylic acid, then 1B can then be treated with a dehydrating agent (such as such as diisopropylcarbodiimide) to form 1E, where E is an amide.

[Scheme 1, Step 1(iv)] Alternatively, if one of the two groups R² or R⁴ is an amine, or substituted alkylamine and the other group is an alkyl group substituted with a leaving group (such as a halogen, or a triflate) then 1B can be treated with a base (such as diisopropylethylamine, pyridine or potassium carbonate) to form 1E, where E is a substituted amine.

[Scheme 1, Step 1(iv)] Alternatively, if one of the two groups R² or R⁴ is an aldehyde, and the other group is a phosphorane (such as an alkyl triphenylphosphorane) or an alkyl phosphonate (such as an alkyl phosphonic acid diethylester) then 1B can be treated with a base (such as diisopropylethylamine, potassium carbonate or sodium hexamethyldisilazide) to form 1E, where E is an alkene which may, or may not be further substituted.

[Scheme 1, Step 1(iv)] Alternatively, if one of the two groups R² or R⁴ is an amine and the other group is an aldehyde group then 1B can be treated with an acid (such as p-toluenesulfoniic acid) or a Lewis acid (such as tin tetrachloride) to give 1E, where E is —CR═N— or —N═CR—.

[Scheme 1, Step 1(ii)] Compounds of the structure 1A can be reacted with 1C′ to form the linker E and give compounds of the structure 1C. The formation of the linker E in compounds with the structure 1C may require a number of steps and the preparation of a number of intermediates, and the use of protecting groups may also be required.

[Scheme 1, Step 1(ii)] For example, if one of the two groups R² or R⁶ is a hydroxyl group and the other group is a substituted alkylalcohol then 1A and 1C′ can be treated with a dehydrating agent (such as diisopropyl azodicarboxylate in the presence of a phosphine, such as triphenylphosphine) to give 1C, where E is an ether. Alternatively, if one of the two groups R² or R⁴ is a hydroxyl and the other group is an alkyl group substituted with a leaving group (such as a halogen, or a triflate) 1A and 1C′ can be treated with a base (such as diisopropylethylamine, potassium carbonate or sodium hydride) to form 1C, where E is an ether.

[Scheme 1, Step 1(ii)] Alternatively, if one of the two groups R² or R⁶ is a hydroxyl, or alkylalcohol and the other group is a carboxylic acid, then the carboxylic acid can be converted to an acyl halide (for example by treatment with thionyl chloride), or to a mixed anhydride (for example by treatment with 2,4,6-trichlorobenzoyl chloride in the presence of a base such as diisopropylethylamine) or to an active ester (for example by treatment with HATU in the presence of a base such as diisopropylethylamine or pyridine, or treatment with diisopropylcarbodiimide in the presence of HOBT), then 1A and 1C′ can be combined to form 1C, where E is an ester.

[Scheme 1, Step 1(ii)] Alternatively, if one of the two groups R² or R⁶ is an amine, or alkylamine and the other group is a carboxylic acid, then the carboxylic acid can be converted to an acyl halide (for example by treatment with thionyl chloride), or to a mixed anhydride (for example by treatment with 2,4,6-trichlorobenzoyl chloride in the presence of a base such as diisopropylethylamine), or to an active ester (for example by treatment with HATU in the presence of disopropylethylamine or pyridine, or treatment with diisopropylcarbodiimide in the presence of HOBT), then 1A and 1C′ can be combined to form 1C, where E is an amide.

[Scheme 1, Step 1(ii)] Alternatively, if one of the two groups R² or R⁶ is an amine, or substituted alkylamine and the other group is an alkyl group substituted with a leaving group (such as a halogen, or a triflate) then 1A and 1C′ can be treated with a base (such as diisopropylethylamine, pyridine or potassium carbonate) to form 1C, where E is a substituted amine.

[Scheme 1, Step 1(ii)] Alternatively, if one of the two groups R² or R⁶ is an aldehyde, and the other group is a phosphorane (such as an alkyltriphenylphosphorane) or an alkylphosphonate (such as an alkylphosphonic acid diethyl ester) then 1A and 1C′ can be treated with a base (such as diisopropylethylamine or potassium carbonate or sodium hexamethyldisilazide) to form 1C, where E is an alkene which may, or may not be further substituted.

[Scheme 1, Step 1(v)] Compounds of structure 1E may be prepared from compounds of structure 1C by reaction of the groups R¹ and R⁵ under a range of conditions to form a carbon-carbon bond. If one of the groups R¹ or R⁵ is a suitable functional group (such as a halide or triflate), and the other group is a borane, boronate or boronic acid then, in the presence of a palladium catalyst (such as palladium chloride dppf adduct), in the presence of a base (such as cesium carbonate), in an appropriate solvent (such as dichloromethane or tetrahydrofuran) and under appropriate conditions (such as heating, for example heating at 80-120° C. for 1-2 hours or microwave irradiation at 120-10° C. for 10 minutes to 1 hour), 1C can be converted into 1E. A wide range of appropriate reagents and conditions are known to those skilled in the art to couple organoboranes, boronates and boronic acids to give 1E.

[Scheme 1, Step 1(v)] Alternatively, if one of the groups R¹ or R⁵ is a suitable leaving group (such as a halide or triflate), and the other group is a trialkylstannane, the carbon-carbon bond can be formed in the presence of a palladium catalyst (such as palladium chloride dppf adduct), in an appropriate solvent (such as dimethoxyethane or tetrahydrofuran) and under appropriate conditions (such as heating, at 80-120° C. for 1-2 hours or by microwave irradiation at 120-160° C. for 10 minutes to 1 hour) to afford 1E. A wide range of appropriate reagents and conditions are known to those skilled in the art to couple heteroaryl stannanes to arylhalides.

[Scheme 1, Step 1(iii)] Compounds of structure 1A may be reacted under a range of conditions with intermediates of the type 1D′ to give compounds of structure 1D, where D is a six- or seven-membered fused heterocyclic ring and R⁹ and R¹⁰ are suitable functional groups that may be used to form the B-ring. The groups R¹ and R⁷ may be reacted together to form a carbon-carbon bond, and the groups R² and R⁸ may be reacted together to form the group E. Methods to form bicyclic compounds of structure 1D from substituted phenyl rings of structure 1A are well known to those skilled in the art (see Comprehensive Heterocyclic Chemistry Ed.: Katritzky, Ramsden, Scriven, and Taylor, Elsevier, 2008). For example, a compound of structure 1A, where R² is a hydroxyl group and R¹ is hydrogen, can be treated with a suitably protected and substituted 3-halo-propanoic acid or ester in an appropriate solvent (such as THF or DMF) and in the presence of a base (such as sodium carbonate or diisopropylethylamine) under appropriate conditions (such as heating, for example to above room temperature or to reflux) to give a compound of the type 1A, where R² is a substituted oxypropanoic acid or ester. This intermediate may be treated with a suitable reagent (such as a strong acid, for example triflic acid) to give 1D where R⁹ is oxo, R¹⁰ is hydrogen and E is —OCH₂—.

The general synthetic strategy used to elaborate 1D is depicted in Scheme 2. Compounds of the structure 1D may be modified by the substitution of groups at R⁹ and R¹⁰ such as alkylation, halogenation, sulfonylation, nitration and formylation. Alternatively, the groups at R⁹ and R¹⁰ may be modified using methods such as reduction (for example the conversion of a nitro group into an amine), oxidation (for example oxidation of an alcohol to an aldehyde or carboxylic acid) or halogenation (for example the conversion of an alcohol into an alkylhalide).

[Scheme 2, Step 2(i)] Compounds of structure 1D may be converted to compounds of structure 1E using a variety of methods known to those skilled in the art to prepare five-membered heterocycles [see Joule, Mills and Smith, Heterocyclic Chemistry, 3^(th) Edition, Chapman and Hall: London, 1995]. For example, where R⁹ is an oxo group and R¹⁰ is an aldehyde, treatment with hydroxylamine under appropriate conditions (such as heating, for example to reflux) in an appropriate solvent (such as pyridine) would convert 1D into 2A where the B ring is an isoxazole.

[Scheme 2, Step 2(ii)] Alternatively, where R⁹ is an aldehyde and R¹⁰ is an oxo group, treatment with hydrazine, which may, or may not, be mono-substituted, under appropriate conditions (such as heating, for example to reflux) in an appropriate solvent (such as pyridine) would convert 1D into 2B where the B ring is a pyrazole.

[Scheme 2, Step 2(iii)] Alternatively, where R⁹ and R¹⁰ are amines, treatment with formic acid under appropriate conditions (such as heating, for example to reflux) in an appropriate solvent (such as an alcohol) would convert 1D into 2C where the B ring is an imidazole.

[Scheme 2, Step 2(iv)] Alternatively, where R⁹ is an amine and R¹⁰ is a hydroxyl, treatment with formic acid under appropriate conditions (such as heating, for example to reflux) in an appropriate solvent (such as an alcohol) would convert 1D into 2D where the B ring is an oxazole.

[Scheme 2, Step 2(v)] Alternatively, where R⁹ is hydrogen and R¹⁰ is a thiol, treatment with 2-bromo-1,1-diethoxyethane in the presence of a base (such as diisopropylethylamine, or sodium carbonate) followed by treatment with a strong acid (such as hydrochloric acid) under appropriate conditions (such as heating, for example to reflux) would convert 1D into 2E where the B ring is a thiophene.

[Scheme 2, Step 2(vi)] Alternatively, where R⁹ is chlorine and R¹⁰ is an aldehyde, treatment with ammonium thiocyanate under appropriate conditions (such as heating, for example to reflux in acetone) would convert 1D into 2F where the B ring is a isothiazole.

Once the group E has been assembled, it may be further modified using methods known to those skilled in the art. For example, if the group E is an alkene, 1E or 1C may be treated with a reducing agent (for example hydrogen) in the presence of an appropriate catalyst (such as palladium on carbon) and the group E converted to an alkane. Alternatively, if the group E is or contains an amide, then 1E or 1C may be treated with a reducing agent (such as borane) in a suitable solvent (such as tetrahydrofuran) under appropriate conditions (such as heating to reflux) and the group E converted to an amine. Alternatively, if the group E is or contains an ester, then 1E may be treated with reducing with an agent such as borane or borane dimethylsulfide to provide 1E where E is an ether.

Alternatively, if the group E is an ethylene group, 1E may be treated with an oxidising agent (such as 2,3-dichloro-5,6-dicyano-p-benzoquinone) in a suitable solvent (such as toluene) under appropriate conditions (such as heating, for example to reflux) and the group E converted to an alkene, such that the ring D is a phenyl ring. Alternatively, if the group E is an amide, then 1E may be treated with a halogenating agent (such as phosphorus trichloride or thionyl chloride) and the group E converted into a chloro-heterocycle, such that the ring D is a 2-chloropyridine. The 2-chloropyridine ring may be further derivatised, for example by treating with an alkoxide (such as sodum ethoxide) in an appropriate solvent (such as THF) to give a 2-alkoxypyridine, or treated with a reducing agent (such as hydrogen) in an appropriate solvent (such as ethanol) in the presence of a suitable catalyst (such as palladium on charcoal) to give a pyridine.

[Scheme 1, Step 1(vii)] Compounds of general structure 1E may be converted to compounds of General Formula I by the conversion of the group F′ to a carboxylic acid. If the group F′ is a carboxylic ester (such as a methyl, t-butyl or benzyl ester) then a variety of reagents and conditions can be used to convert 1E into a compound of the General Formula I.

[Scheme 1, Step 1(vii)] Alternatively, if the group F′ is a nitrile, it may be converted into a carboxylic acid by treatment with aqueous acid (such as a mineral acid, for example hydrochloric acid) under appropriate conditions (such as heating, for example to reflux); or by treatment with aqueous base (such as an aqueous hydroxide, for example aqueous sodium hydroxide) under appropriate conditions (such as heating, for example to reflux).

[Scheme 1, Step 1(vii)] Alternatively, if the group F′ is an aldehyde (—CHO) or a hydroxymethyl (—CH₂OH) moiety then it may be converted into a carboxylic acid by treatment with a suitable oxidising reagent (such as potassium permanganate or chromic acid).

The general synthetic strategy used to modify the group F is depicted in Schemes 3 and 4. The group F may be introduced and/or modified either before, after or whilst the tricyclic ring system is assembled as depicted in Scheme 1. Specific steps in the synthetic process used to assemble the group F are described in more detail below.

When the group Y in Formula I is —C(R^(Y1)R^(Y2)), the group F may be introduced and modified as shown in Scheme 3. The asterix denote either the presence of R¹ and R² (as per Scheme 1) or the presence of the D and B rings, or their precursors.

[Scheme 3, Step 3 (i)] When LG¹ is a suitable leaving group (such as a halide, triflate or tosylate), compounds of the structure 3A can be treated with an appropriate thiol (such as an arylthiol, heteroaryl thiol, or heterocyclyl thiol) in the presence of a base (such as potassium carbonate, or sodium hydride) in an appropriate solvent (such as DMF or ethanol) and under appropriate conditions (such as heating, for example to 80-120° C. for 1-6 hours, or at room temperature) to give the thioether 3B. A wide range of appropriate reagents and conditions are known to those skilled in the art to convert 3A to the thioether 3B. [for example, see Peach in Patai The Chemistry of the Thiol Group, pt2; Wiley: New York, 1974, pp. 721]

[Scheme 3, Step 3 (ii)] In Step 3(ii), structure 3B can be treated with an oxidising agent (such as 3-chloroperbenzoic acid) in a suitable solvent (such as dichloromethane) under suitable conditions (for example at room temperature or below) to give the sulfinyl derivative 3C (n=1). Alternatively, 3B can be treated with an oxidising agent (such as hydrogen peroxide) in a suitable solvent (such as acetic acid) and under appropriate conditions (such as heating, for example to 50-100° C. for 1-6 hours) to afford the sulfonyl derivative 3C (n=2). A wide range of appropriate reagents and conditions are known to those skilled in the art to oxidise 3B to 3C. [For example, see Drabowicz, Kielbasinski, Mikolajczyk in Patai, Rappoport, Stirling The Chemistry of Sulfones and Sulfoxides; Wiley: New York, 1988, pp. 233-378, pp 235-255. Madesclaire Tetrahedron 1986, 42, 549-5495. Oae The Organic Chemistry of Sulfur; Plenum: New York 1977, pp. 385-390. Smith, March, March's Advanced Organic Chemistry, 5^(th) Edition, Wiley: New York, 2001, pp. 1541-1542].

[Scheme 3, Step 3 (iii)] Structure 3D of Step 3(iii) can optionally be treated with an alkylating agent (such as an alkyl halide, alkyltriflate or alkylsulfate which may, or may not be further substituted) in the presence of a base (such as sodium hydride, lithium hexamethyldisilazide or lithium diisopropylamine), in an appropriate solvent (such as dimethylformamide or tetrahydrofuran) and under appropriate conditions (such as room temperature or below, for example 0° C.) to afford 3C. A wide range of appropriate reagents and conditions are known to those skilled in the art to monoalkylate 3D to afford 3C (R⁷ or R⁸=H), or to dialkylate 3D to afford 3C (R⁷ and R⁸≠H). [Smith, March, March's Advanced Organic Chemistry, 5^(th) Edition, Wiley: New York, 2001, pp. 548-551]

[Scheme 3, Step 3 (iv) (v)] Compounds of the type 3A can be treated with sodium sulfite in an appropriate solvent (such as water, tetrahydrofuran) to afford an alkylsulfonic acid which can be treated with a chlorinating agent (such as phosphorous pentachloride or thionyl chloride) to afford 3E (LG²=Cl, n=2). 3E can then be treated with a cyclic amine (such as piperidine or morpholine) in an appropriate solvent (such as pyridine or dimethylformamide) in the presence of a base (such as diisopropylethylamine or cesium carbonate) to afford 3C, in which A is an N-linked heterocycle, as depicted in Step 3(v).

[Scheme 3, Step 3 (vi)] Compounds of the type 3A can be treated with an appropriate sulfinate (such as an arylsulfinate, heteroaryl sulfinate or heterocyclyl sulfinate) in the presence of a base (such as sodium bicarbonate, potassium carbonate, or diisopropylethylamine) in an appropriate solvent (such as dimethylacetamide/water) and under appropriate conditions (such as heating, for example to 80-120° C. for 1-6 hours), to give the sulfone 3C (n=2).

When the group Y in Formula I is —N(R^(Y3))—, the group F may be introduced and modified as shown in Scheme 4. The asterix denote either the presence of R¹ and R² (as per Scheme 1), or the presence of the D and B rings, or their precursors.

[Scheme 4, Step 4(i)] Compounds of structure 4A can be converted into 4B by treatment with a sulfonyl chloride (such as a substituted benzenesulfonyl chloride) or an activated sulfonyl ester (such as a pentafluorophenylsulfonyl ester) in a suitable organic solvent (such as DMF or dichloromethane), in the presence of a suitable base (such as pyridine, diisopropylethylamine or caesium carbonate) and under appropriate conditions (such as heating, for example to 50-100° C. for 1-6 hours).

[Scheme 4, Step 4(ii)] Compounds of structure 4B can be converted into 4C by treatment with an alkylation agent (such as an alkylhalide, alkyltriflate or alkylsulfate which may, or may not, be further substituted) in the presence of a base (such as sodium hydride or lithium hexamethyldisilazide) in an appropriate solvent (such as dimethylformamide or tetrahydrofuran) and under appropriate conditions (such as room temperature or below, for example 0° C.).

Compounds of any of Formula I or for example, General Formula I as depicted above, or any of the intermediates described in the schemes above, can be further derivatised by using one or more standard synthetic methods known to those skilled in the art. Such methods can involve substitution, oxidation or reduction reactions. These methods can also be used to obtain or modify compounds of General Formula I or any preceding intermediates by modifying, introducing or removing appropriate functional groups. Particular substitution approaches include alkylation, arylation, heteroarylation, acylation, thioacylation, halogenation, sulfonylation, nitration, formylation, hydrolysis and coupling procedures. These procedures can be used to introduce a functional group onto the parent molecule (such as the nitration or sulfonylation of aromatic rings) or to couple two molecules together (for example to couple an amine to a carboxylic acid to afford an amide; or to form a carbon-carbon bond between two heterocycles). For example, alcohol or phenol groups can be converted to ether groups by coupling a phenol with an alcohol in a solvent such as tetrahydrofuran in the presence of a phosphine (such as triphenylphosphine) and a dehydrating agent (such as diethyl, diisopropyl or dimethyl azodicarboxylate). Alternatively, ether groups can be prepared by deprotonation of an alcohol, using a suitable base (such as sodium hydride) followed by the addition of an alkylating agent (such as an alkyl halide or an alkylsulfonate).

In another example, a primary or secondary amine can be alkylated using a reductive alkylation process. For example, the amine can be treated with an aldehyde and a borohydride (such as sodium triacetoxyborohydride, or sodium cyanoborohydride in a solvent (such as a halogenated hydrocarbon, for example dichloromethane, or an alcohol, for example ethanol) and, where necessary, in the presence of an acid (such as acetic acid).

In another example, hydroxy groups (including phenolic OH groups) can be converted into leaving groups such as halogen atoms or sulfonyloxy groups (such as alkylsulfonyloxy, for example trifluoromethylsulfonyloxy, or arylsuphonyl, for example p-toluenesulfonyloxy) using conditions known to those skilled in the art. For example, an aliphatic alcohol can be reacted with thionyl chloride in a halogenated hydrocarbon (such as dichloromethane) to afford the corresponding alkylchloride. A base (such as triethylamine) can also be used in the reaction.

In another example, ester groups can be converted to the corresponding carboxylic acid by acid- or base-catalysed hydrolysis depending on the nature of the ester group. Acid catalysed hydrolysis can be achieved by treatment with an organic or inorganic acid (such as trifluoroacetic acid in an aqueous solvent, or a mineral acid such as hydrochloric acid in a solvent such as dioxan). Base catalysed hydrolysis can be achieved by treatment with an alkali metal hydroxide (such as lithium hydroxide in an aqueous alcohol, for example methanol).

In another example, aromatic halogen substituents in the compounds may be subjected to halogen-metal exchange by treatment with a base (such as a lithium base, for example n-butyl or t-butyl lithium) optionally at a low temperature (such as −78° C.) in a solvent (such as tetrahydrofuran) and the mixture may then be quenched with an electrophile to introduce a desired substituent. Thus, for example, a formyl group can be introduced by using dimethylformamide as the electrophile. Aromatic halogen substituents can also be subjected to palladium catalysed reactions to introduce groups such as carboxylic acids, esters, cyano or amino substituents.

In another example, an aryl, or heteroaryl ring substituted with an appropriate leaving group (such as a halogen or sulfonyl ester, for example a triflate) can undergo a palladium catalysed coupling reaction with a wide variety of substrates to form a carbon-carbon bond. For example, a Heck reaction can be used to couple such a ring system to an alkene (which may, or may not, be further substituted) by treatment with an organopalladium complex (such as tetrakis(triphenylphosphine)palladium(0), palladium (II) acetate or palladium (II) chloride) in the presence of a ligand (such as a phosphine, for example triphenylphosphine) in the presence of a base (such as potassium carbonate or a tertiary amine, for example, triethylamine), in an appropriate solvent (such as tetrahydrofuran or DMF), under appropriate conditions (such as heating to, for example, 50-120° C.). In another example, a Sonogashira reaction can be used to couple such a ring system to an alkyne (which may, or may not be further substituted) by treatment with a palladium complex (such as tetrakis(triphenylphosphine)palladium(0)) and a halide salt of copper (I) (such as copper (I) iodide), in the presence of a base (such as a potassium carbonate or a tertiary amine, for example, triethylamine), in an appropriate solvent (such as tetrahydrofuran or DMF), under appropriate conditions (such as heating to, for example, 50-120° C.). In another example, a Stille reaction can be used to couple such a ring system to an alkene, by treatment with an organotin compound (such as an alkynyltin or alkenyltin reagent, for example an alkenyltributylstannane) in the presence of a palladium complex (such as tetrakis(triphenylphosphine)palladium(0)), with, or without the presence of a salt (such as a copper (I) halide), in an appropriate solvent (such as dioxane or DMF), under appropriate conditions (such as heating to, for example, 50-120° C.).

Particular oxidation approaches include dehydrogenations and aromatisation, decarboxylation and the addition of oxygen to certain functional groups. For example, aldehyde groups can be prepared by oxidation of the corresponding alcohol using conditions well known to those skilled in the art. For example, an alcohol can be treated with an oxidising agent (such as the Dess-Martin reagent) in a solvent (such as a halogenated hydrocarbon, for example dichloromethane). Alternative oxidising conditions can be used, such as treatment with oxalyl chloride and an activating amount of dimethylsulfoxide and subsequent quenching by the addition of an amine (such as triethylamine). Such a reaction can be carried out in an appropriate solvent (such as a halogenated hydrocarbon, for example dichloromethane) and under appropriate conditions (such as cooling below room temperature, for example to −78° C. followed by warming to room temperature). In another example, sulfur atoms can be oxidised to the corresponding sulfoxide or sulfone using an oxidising agent (such as a peroxy acid, for example 3-chloroperoxybenzoic acid) in an inert solvent (such as a halogenated hydrocarbon, for example dichloromethane) at around ambient temperature.

Particular reduction approaches include the removal of oxygen atoms from particular functional groups, saturation (or partial saturation) of unsaturated compounds including aromatic rings. For example, primary alcohols can be generated from the corresponding ester or aldehyde by reduction, using a metal hydride (such as lithium aluminium hydride or sodium borohydride in a solvent such as methanol). Alternatively, —CH₂OH groups can be generated from the corresponding carboxylic acid by reduction, using a metal hydride (such as lithium aluminium hydride in a solvent such as tetrahydrofuran). In another example, a nitro group may be reduced to an amine by catalytic hydrogenation in the presence of a metal catalyst (such as palladium on a solid support such as carbon) in a solvent (such as an ether, for example tetrahydrofuran, or an alcohol, such as methanol), or by chemical reduction using a metal (such as tin or iron) in the presence of an acid (such as hydrochloric acid). In a further example an amine can be obtained by reduction of a nitrile, for example by catalytic hydrogenation in the presence of a metal catalyst (such as palladium on a solid support such as carbon), or Raney nickel in a solvent (such as tetrahydrofuran) and under suitable conditions (such as cooling to below room temperature, for example to −78° C., or heating, for example to reflux).

Salts of compounds of General Formula I can be prepared by the reaction of a compound of General Formula I with an appropriate acid or base in a suitable solvent, or mixture of solvents (such as an ether, for example, diethylether, or an alcohol, for example ethanol, or an aqueous solvent) using conventional procedures. Salts of compound of General Formula I can be exchanged for other salts by treatment using conventional ion-exchange chromatography procedures.

Where it is desired to obtain a particular enantiomer of a compound of General Formula I, this may be produced from a corresponding mixture of enantiomers by employing any suitable conventional procedure for resolving enantiomers. For example, diastereomeric derivatives (such as salts) can be produced by reaction of a mixture of enantiomers of a compound of General Formula I (such a racemate) and an appropriate chiral compound (such as a chiral base). The diastereomers can then be separated by any conventional means such as crystallisation, and the desired enantiomer recovered (such as by treatment with an acid in the instance where the diastereomer is a salt). Alternatively, a racemic mixture of esters can be resolved by kinetic hydrolysis using a variety of biocatalysts (for example, see Patel Steroselective Biocatalysts, Marcel Decker; New York 2000).

In another resolution process a racemate of compounds of General Formula I can be separated using chiral High Performance Liquid Chromatography. Alternatively, a particular enantiomer can be obtained by using an appropriate chiral intermediate in one of the processes described above. Chromatography, recrystallisation and other conventional separation procedures may also be used with intermediates or final products where it is desired to obtain a particular geometric isomer of the invention.

II. Methods

Another aspect of the invention provides methods of modulating the activity of MetAP2. Such methods comprise exposing said receptor to a compound described herein. In some embodiments, the compound utilized by one or more of the foregoing methods is one of the generic, subgeneric, or specific compounds described herein, such as a compound of Formula I, IIa, IIb, IIc, or III. The ability of compounds described herein to modulate or inhibit MetAP2 can be evaluated by procedures known in the art and/or described herein. Another aspect of the invention provides methods of treating a disease associated with expression or activity of MetAP2 in a patient. For example, a contemplated method includes administering a disclosed compound in an amount sufficient to establish inhibition of intracellular MetAP2 effective to increase thioredoxin production in the patient and to induce multi organ stimulation of anti-obesity processes in the subject, for example, by administering a disclosed compound in an amount insufficient to reduce angiogenesis in the patient.

In certain embodiments, the invention provides a method of treating and or ameliorating obesity in a patient by administering an effective amount of a disclosed compound. Also provided herein are methods for inducing weight loss in a patient in need thereof. Contemplated patients include not only humans, but other animals such as companion animals (e.g., dogs, cats).

Other contemplated methods of treatment include method of treating or ameliorating an obesity-related condition or co-morbidity, by administering a compound disclosed herein to a subject. For example, contemplated herein are methods for treating type 2 diabetes in a patient in need thereof.

Exemplary co-morbidities include cardiac disorders, endocrine disorders, respiratory disorders, hepatic disorders, skeletal disorders, psychiatric disorders, metabolic disorders, and reproductive disorders.

Exemplary cardiac disorders include hypertension, dyslipidemia, ischemic heart disease, cardiomyopathy, cardiac infarction, stroke, venous thromboembolic disease and pulmonary hypertension. Exemplary endocrine disorders include type 2 diabetes and latent autoimmune diabetes in adults. Exemplary respiratory disorders include obesity-hypoventilation syndrome, asthma, and obstructive sleep apnea. An exemplary hepatic disorder is nonalcoholic fatty liver disease. Exemplary skeletal disorders include back pain and osteoarthritis of weight-bearing joints. Exemplary metabolic disorders include Prader-Willi Syndrome and polycystic ovary syndrome. Exemplary reproductive disorders include sexual dysfunction, erectile dysfunction, infertility, obstetric complications, and fetal abnormalities. Exemplary psychiatric disorders include weight-associated depression and anxiety.

In particular, in certain embodiments, the invention provides a method of treating the above medical indications comprising administering to a subject in need thereof a therapeutically effective amount of a compound described herein, such as a compound of Formula I, IIa, IIb, IIc, or III.

Obesity or reference to “overweight” refers to an excess of fat in proportion to lean body mass. Excess fat accumulation is associated with increase in size (hypertrophy) as well as number (hyperplasia) of adipose tissue cells. Obesity is variously measured in terms of absolute weight, weight:height ratio, distribution of subcutaneous fat, and societal and esthetic norms. A common measure of body fat is Body Mass Index (BMI). The BMI refers to the ratio of body weight (expressed in kilograms) to the square of height (expressed in meters). Body mass index may be accurately calculated using either of the formulas: weight(kg)/height²(m²) (SI) or 703×weight(lb)/height²(in²) (US).

In accordance with the U.S. Centers for Disease Control and Prevention (CDC), an overweight adult has a BMI of 25 kg/m² to 29.9 kg/m², and an obese adult has a BMI of 30 kg/m² or greater. A BMI of 40 kg/m² or greater is indicative of morbid obesity or extreme obesity. Obesity can also refer to patients with a waist circumference of about 102 cm for males and about 88 cm for females. For children, the definitions of overweight and obese take into account age and gender effects on body fat. Patients with differing genetic background may be considered “obese” at a level differing from the general guidelines, above.

The compounds of the present invention also are useful for reducing the risk of secondary outcomes of obesity, such as reducing the risk of left ventricular hypertrophy. Methods for treating patients at risk of obesity, such as those patients who are overweight, but not obese, e.g. with a BMI of between about 25 and 30 kg/m², are also contemplated. In certain embodiments, a patient is a human.

BMI does not account for the fact that excess adipose can occur selectively in different parts of the body, and development of adipose tissue can be more dangerous to health in some parts of the body rather than in other parts of the body. For example, “central obesity”, typically associated with an “apple-shaped” body, results from excess adiposity especially in the abdominal region, including belly fat and visceral fat, and carries higher risk of co-morbidity than “peripheral obesity”, which is typically associated with a “pear-shaped” body resulting from excess adiposity especially on the hips. Measurement of waist/hip circumference ratio (WHR) can be used as an indicator of central obesity. A minimum WHR indicative of central obesity has been variously set, and a centrally obese adult typically has a WHR of about 0.85 or greater if female and about 0.9 or greater if male.

Methods of determining whether a subject is overweight or obese that account for the ratio of excess adipose tissue to lean body mass involve obtaining a body composition of the subject. Body composition can be obtained by measuring the thickness of subcutaneous fat in multiple places on the body, such as the abdominal area, the subscapular region, arms, buttocks and thighs. These measurements are then used to estimate total body fat with a margin of error of approximately four percentage points. Another method is bioelectrical impedance analysis (BIA), which uses the resistance of electrical flow through the body to estimate body fat. Another method is using a large tank of water to measure body buoyancy. Increased body fat will result in greater buoyancy, while greater muscle mass will result in a tendency to sink.

In another aspect, the invention provides methods for treating an overweight or obese subject involving determining a level of at least one biomarker related to being overweight or obese in the subject, and administering an effective amount of a disclosed compound to achieve a target level in the subject. Exemplary biomarkers include body weight, Body Mass Index (BMI), Waist/Hip ratio WHR, plasma adipokines, and a combination of two or more thereof.

In certain embodiments, the compound utilized by one or more of the foregoing methods is one of the generic, subgeneric, or specific compounds described herein, such as a compound of Formula I, IIa, IIb, IIc, or III.

The compounds of the invention may be administered to patients (animals and humans) in need of such treatment in dosages that will provide optimal pharmaceutical efficacy. It will be appreciated that the dose required for use in any particular application will vary from patient to patient, not only with the particular compound or composition selected, but also with the route of administration, the nature of the condition being treated, the age and condition of the patient, concurrent medication or special diets then being followed by the patient, and other factors which those skilled in the art will recognize, with the appropriate dosage ultimately being at the discretion of the attendant physician. For treating clinical conditions and diseases noted above, a compound of this invention may be administered orally, subcutaneously, topically, parenterally, by inhalation spray or rectally in dosage unit formulations containing conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles. Parenteral administration may include subcutaneous injections, intravenous or intramuscular injections or infusion techniques.

Treatment can be continued for as long or as short a period as desired. The compositions may be administered on a regimen of, for example, one to four or more times per day. A suitable treatment period can be, for example, at least about one week, at least about two weeks, at least about one month, at least about six months, at least about 1 year, or indefinitely. A treatment period can terminate when a desired result, for example a weight loss target, is achieved. A treatment regimen can include a corrective phase, during which dose sufficient to provide reduction of weight is administered, and can be followed by a maintenance phase, during which a e.g. a lower dose sufficient to prevent weight gain is administered. A suitable maintenance dose is likely to be found in the lower parts of the dose ranges provided herein, but corrective and maintenance doses can readily be established for individual subjects by those of skill in the art without undue experimentation, based on the disclosure herein. Maintenance doses can be employed to maintain body weight in subjects whose body weight has been previously controlled by other means, including diet and exercise, bariatric procedures such as bypass or banding surgeries, or treatments employing other pharmacological agents.

III. Pharmaceutical Compositions and Kits

Another aspect of the invention provides pharmaceutical compositions comprising compounds as disclosed herein formulated together with a pharmaceutically acceptable carrier. In particular, the present disclosure provides pharmaceutical compositions comprising compounds as disclosed herein formulated together with one or more pharmaceutically acceptable carriers. These formulations include those suitable for oral, rectal, topical, buccal, parenteral (e.g., subcutaneous, intramuscular, intradermal, or intravenous) rectal, vaginal, or aerosol administration, although the most suitable form of administration in any given case will depend on the degree and severity of the condition being treated and on the nature of the particular compound being used. For example, disclosed compositions may be formulated as a unit dose, and/or may be formulated for oral or subcutaneous administration.

Exemplary pharmaceutical compositions of this invention may be used in the form of a pharmaceutical preparation, for example, in solid, semisolid or liquid form, which contains one or more of the compound of the invention, as an active ingredient, in admixture with an organic or inorganic carrier or excipient suitable for external, enteral or parenteral applications. The active ingredient may be compounded, for example, with the usual non-toxic, pharmaceutically acceptable carriers for tablets, pellets, capsules, suppositories, solutions, emulsions, suspensions, and any other form suitable for use. The active object compound is included in the pharmaceutical composition in an amount sufficient to produce the desired effect upon the process or condition of the disease.

For preparing solid compositions such as tablets, the principal active ingredient may be mixed with a pharmaceutical carrier, e.g., conventional tableting ingredients such as corn starch, lactose, sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalcium phosphate or gums, and other pharmaceutical diluents, e.g., water, to form a solid preformulation composition containing a homogeneous mixture of a compound of the invention, or a non-toxic pharmaceutically acceptable salt thereof. When referring to these preformulation compositions as homogeneous, it is meant that the active ingredient is dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective unit dosage forms such as tablets, pills and capsules.

In solid dosage forms for oral administration (capsules, tablets, pills, dragees, powders, granules and the like), the subject composition is mixed with one or more pharmaceutically acceptable carriers, such as sodium citrate or dicalcium phosphate, and/or any of the following: (1) fillers or extenders, such as starches, lactose, sucrose, glucose, mannitol, and/or silicic acid; (2) binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose and/or acacia; (3) humectants, such as glycerol; (4) disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; (5) solution retarding agents, such as paraffin; (6) absorption accelerators, such as quaternary ammonium compounds; (7) wetting agents, such as, for example, acetyl alcohol and glycerol monostearate; (8) absorbents, such as kaolin and bentonite clay; (9) lubricants, such a talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof; and (10) coloring agents. In the case of capsules, tablets and pills, the compositions may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like.

A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared using binder (for example, gelatin or hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (for example, sodium starch glycolate or cross-linked sodium carboxymethyl cellulose), surface-active or dispersing agent. Molded tablets may be made by molding in a suitable machine a mixture of the subject composition moistened with an inert liquid diluent. Tablets, and other solid dosage forms, such as dragees, capsules, pills and granules, may optionally be scored or prepared with coatings and shells, such as enteric coatings and other coatings well known in the pharmaceutical-formulating art.

Compositions for inhalation or insufflation include solutions and suspensions in pharmaceutically acceptable, aqueous or organic solvents, or mixtures thereof, and powders. Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the subject composition, the liquid dosage forms may contain inert diluents commonly used in the art, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, cyclodextrins and mixtures thereof.

Suspensions, in addition to the subject composition, may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.

Formulations for rectal or vaginal administration may be presented as a suppository, which may be prepared by mixing a subject composition with one or more suitable non-irritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate, and which is solid at room temperature, but liquid at body temperature and, therefore, will melt in the body cavity and release the active agent.

Dosage forms for transdermal administration of a subject composition include powders, sprays, ointments, pastes, creams, lotions, gels, solutions, patches and inhalants. The active component may be mixed under sterile conditions with a pharmaceutically acceptable carrier, and with any preservatives, buffers, or propellants which may be required.

The ointments, pastes, creams and gels may contain, in addition to a subject composition, excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Powders and sprays may contain, in addition to a subject composition, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays may additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane.

Compositions and compounds of the present invention may alternatively be administered by aerosol. This is accomplished by preparing an aqueous aerosol, liposomal preparation or solid particles containing the compound. A non-aqueous (e.g., fluorocarbon propellant) suspension could be used. Sonic nebulizers may be used because they minimize exposing the agent to shear, which may result in degradation of the compounds contained in the subject compositions. Ordinarily, an aqueous aerosol is made by formulating an aqueous solution or suspension of a subject composition together with conventional pharmaceutically acceptable carriers and stabilizers. The carriers and stabilizers vary with the requirements of the particular subject composition, but typically include non-ionic surfactants (Tweens, Pluronics, or polyethylene glycol), innocuous proteins like serum albumin, sorbitan esters, oleic acid, lecithin, amino acids such as glycine, buffers, salts, sugars or sugar alcohols. Aerosols generally are prepared from isotonic solutions.

Pharmaceutical compositions of this invention suitable for parenteral administration comprise a subject composition in combination with one or more pharmaceutically-acceptable sterile isotonic aqueous or non-aqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents.

Examples of suitable aqueous and non-aqueous carriers which may be employed in the pharmaceutical compositions of the invention include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate and cyclodextrins. Proper fluidity may be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants

In another aspect, the invention provides enteral pharmaceutical formulations including a disclosed compound and an enteric material; and a pharmaceutically acceptable carrier or excipient thereof. Enteric materials refer to polymers that are substantially insoluble in the acidic environment of the stomach, and that are predominantly soluble in intestinal fluids at specific pHs. The small intestine is the part of the gastrointestinal tract (gut) between the stomach and the large intestine, and includes the duodenum, jejunum, and ileum. The pH of the duodenum is about 5.5, the pH of the jejunum is about 6.5 and the pH of the distal ileum is about 7.5. Accordingly, enteric materials are not soluble, for example, until a pH of about 5.0, of about 5.2, of about 5.4, of about 5.6, of about 5.8, of about 6.0, of about 6.2, of about 6.4, of about 6.6, of about 6.8, of about 7.0, of about 7.2, of about 7.4, of about 7.6, of about 7.8, of about 8.0, of about 8.2, of about 8.4, of about 8.6, of about 8.8, of about 9.0, of about 9.2, of about 9.4, of about 9.6, of about 9.8, or of about 10.0. Exemplary enteric materials include cellulose acetate phthalate (CAP), hydroxypropyl methylcellulose phthalate (HPMCP), polyvinyl acetate phthalate (PVAP), hydroxypropyl methylcellulose acetate succinate (HPMCAS), cellulose acetate trimellitate, hydroxypropyl methylcellulose succinate, cellulose acetate succinate, cellulose acetate hexahydrophthalate, cellulose propionate phthalate, cellulose acetate maleate, cellulose acetate butyrate, cellulose acetate propionate, copolymer of methyl methacrylic acid and methyl methacrylate, copolymer of methyl acrylate, methylmethacrylate and methacrylic acid, copolymer of methylvinyl ether and maleic anhydride (Gantrez ES series), ethyl methyacrylate-methylmethacrylate-chlorotrimethylammonium ethyl acrylate copolymer, natural resins such as zein, shellac and copal collophorium, and several commercially available enteric dispersion systems (e.g., Eudragit L30D55, Eudragit FS30D, Eudragit L100, Eudragit S100, Kollicoat EMM30D, Estacryl 30D, Coateric, and Aquateric). The solubility of each of the above materials is either known or is readily determinable in vitro. The foregoing is a list of possible materials, but one of skill in the art with the benefit of the disclosure would recognize that it is not comprehensive and that there are other enteric materials that would meet the objectives of the present invention.

Advantageously, the invention also provides kits for use by a e.g. a consumer in need of weight loss. Such kits include a suitable dosage form such as those described above and instructions describing the method of using such dosage form to mediate, reduce or prevent inflammation. The instructions would direct the consumer or medical personnel to administer the dosage form according to administration modes known to those skilled in the art. Such kits could advantageously be packaged and sold in single or multiple kit units. An example of such a kit is a so-called blister pack. Blister packs are well known in the packaging industry and are being widely used for the packaging of pharmaceutical unit dosage forms (tablets, capsules, and the like). Blister packs generally consist of a sheet of relatively stiff material covered with a foil of a preferably transparent plastic material. During the packaging process recesses are formed in the plastic foil. The recesses have the size and shape of the tablets or capsules to be packed. Next, the tablets or capsules are placed in the recesses and the sheet of relatively stiff material is sealed against the plastic foil at the face of the foil which is opposite from the direction in which the recesses were formed. As a result, the tablets or capsules are sealed in the recesses between the plastic foil and the sheet. Preferably the strength of the sheet is such that the tablets or capsules can be removed from the blister pack by manually applying pressure on the recesses whereby an opening is formed in the sheet at the place of the recess. The tablet or capsule can then be removed via said opening.

It may be desirable to provide a memory aid on the kit, e.g., in the form of numbers next to the tablets or capsules whereby the numbers correspond with the days of the regimen which the tablets or capsules so specified should be ingested. Another example of such a memory aid is a calendar printed on the card, e.g., as follows “First Week, Monday, Tuesday, . . . etc. . . . Second Week, Monday, Tuesday, . . . ” etc. Other variations of memory aids will be readily apparent. A “daily dose” can be a single tablet or capsule or several pills or capsules to be taken on a given day. Also, a daily dose of a first compound can consist of one tablet or capsule while a daily dose of the second compound can consist of several tablets or capsules and vice versa. The memory aid should reflect this.

Also contemplated herein are methods and compositions that include a second active agent, or administering a second active agent. For example, in addition to being overweight or obese, a subject or patient can further have overweight- or obesity-related co-morbidities, i.e., diseases and other adverse health conditions associated with, exacerbated by, or precipitated by being overweight or obese. Contemplated herein are disclosed compounds in combination with at least one other agent that has previously been shown to treat these overweight- or obesity-related conditions.

For example, Type II diabetes has been associated with obesity. Certain complications of Type II diabetes, e.g., disability and premature death, can be prevented, ameliorated, or eliminated by sustained weight loss (Astrup, A. Pub Health Nutr (2001) 4:499-5 15). Agents administered to treat Type II diabetes include sulfonylureas (e.g., Chlorpropamide, Glipizide, Glyburide, Glimepiride); meglitinides (e.g., Repaglinide and Nateglinide); biguanides (e.g., Metformin); thiazolidinediones (Rosiglitazone, Troglitazone, and Pioglitazone); dipeptidylpeptidase-4 inhibitors (e.g., Sitagliptin, Vildagliptin, and Saxagliptin); glucagon-like peptide-1 mimetics (e.g., Exenatide and Liraglutide); and alpha-glucosidase inhibitors (e.g., Acarbose and Miglitol.

Cardiac disorders and conditions, for example hypertension, dyslipidemia, ischemic heart disease, cardiomyopathy, cardiac infarction, stroke, venous thromboembolic disease and pulmonary hypertension, have been linked to overweight or obesity. For example, hypertension has been linked to obesity because excess adipose tissue secretes substances that are acted on by the kidneys, resulting in hypertension. Additionally, with obesity there are generally higher amounts of insulin produced (because of the excess adipose tissue) and this excess insulin also elevates blood pressure. A major treatment option of hypertension is weight loss. Agents administered to treat hypertension include Chlorthalidone; Hydrochlorothiazide; Indapamide, Metolazone; loop diuretics (e.g., Bumetanide, Ethacrynic acid, Furosemide, Lasix, Torsemide); potassium-sparing agents (e.g., Amiloride hydrochloride, benzamil, Spironolactone, and Triamterene); peripheral agents (e.g., Reserpine); central alpha-agonists (e.g., Clonidine hydrochloride, Guanabenz acetate, Guanfacine hydrochloride, and Methyldopa); alpha-blockers (e.g., Doxazosin mesylate, Prazosin hydrochloride, and Terazosin hydrochloride); beta-blockers (e.g., Acebutolol, Atenolol, Betaxolol, Bisoprolol fumarate, Carteolol hydrochloride, Metoprolol tartrate, Metoprolol succinate, Nadolol, Penbutolol sulfate, Pindolol, Propranolol hydrochloride, and Timolol maleate); combined alpha- and beta-blockers (e.g., Carvedilol and Labetalol hydrochloride); direct vasodilators (e.g., Hydralazine hydrochloride and Minoxidil); calcium antagonists (e.g., Diltiazem hydrochloride and Verapamil hydrochloride); dihydropyridines (e.g., Amlodipine besylate, Felodipine, Isradipine, Nicardipine, Nifedipine, and Nisoldipine); ACE inhibitors (benazepril hydrochloride, Captopril, Enalapril maleate, Fosinopril sodium, Lisinopril, Moexipril, Quinapril hydrochloride, Ramipril, Trandolapril); Angiotensin II receptor blockers (e.g., Losartan potassium, Valsartan, and Irbesartan); Renin inhibitors (e.g., Aliskiren); and combinations thereof. These compounds are administered in regimens and at dosages known in the art.

Carr et al. (The Journal of Clinical Endocrinology & Metabolism (2004) Vol. 89, No. 6 2601-2607) discusses a link between being overweight or obese and dyslipidemia. Dyslipidemia is typically treated with statins. Statins, HMG-CoA reductase inhibitors, slow down production of cholesterol in a subject and/or remove cholesterol buildup from arteries. Statins include mevastatin, lovastatin, pravastatin, simvastatin, velostatin, dihydrocompactin, fluvastatin, atorvastatin, dalvastatin, carvastatin, crilvastatin, bevastatin, cefvastatin, rosuvastatin, pitavastatin, and glenvastatin. These compounds are administered in regimens and at dosages known in the art. Eckel (Circulation (1997) 96:3248-3250) discusses a link between being overweight or obese and ischemic heart disease. Agents administered to treat ischemic heart disease include statins, nitrates (e.g., Isosorbide Dinitrate and Isosorbide Mononitrate), beta-blockers, and calcium channel antagonists. These compounds are administered in regimens and at dosages known in the art.

Wong et al. (Nature Clinical Practice Cardiovascular Medicine (2007) 4:436-443) discusses a link between being overweight or obese and cardiomyopathy. Agents administered to treat cardiomyopathy include inotropic agents (e.g., Digoxin), diuretics (e.g., Furosemide), ACE inhibitors, calcium antagonists, anti-arrhythmic agents (e.g., Sotolol, Amiodarone and Disopyramide), and beta-blockers. These compounds are administered in regimens and at dosages known in the art. Yusef et al. (Lancet (2005) 366(9497):1640-1649) discusses a link between being overweight or obese and cardiac infarction. Agents administered to treat cardiac infarction include ACE inhibitors, Angiotensin II receptor blockers, direct vasodilators, beta blockers, anti-arrhythmic agents and thrombolytic agents (e.g., Alteplase, Retaplase, Tenecteplase, Anistreplase, and Urokinase). These compounds are administered in regimens and at dosages known in the art.

Suk et al. (Stroke (2003) 34:1586-1592) discusses a link between being overweight or obese and strokes. Agents administered to treat strokes include anti-platelet agents (e.g., Aspirin, Clopidogrel, Dipyridamole, and Ticlopidine), anticoagulant agents (e.g., Heparin), and thrombolytic agents. Stein et al. (The American Journal of Medicine (2005) 18(9):978-980) discusses a link between being overweight or obese and venous thromboembolic disease. Agents administered to treat venous thromboembolic disease include anti-platelet agents, anticoagulant agents, and thrombolytic agents. Sztrymf et al. (Rev Pneumol Clin (2002) 58(2):104-10) discusses a link between being overweight or obese and pulmonary hypertension. Agents administered to treat pulmonary hypertension include inotropic agents, anticoagulant agents, diuretics, potassium (e.g., K-dur), vasodilators (e.g., Nifedipine and Diltiazem), Bosentan, Epoprostenol, and Sildenafil. Respiratory disorders and conditions such as obesity-hypoventilation syndrome, asthma, and obstructive sleep apnea, have been linked to being overweight or obese. Elamin (Chest (2004) 125:1972-1974) discusses a link between being overweight or obese and asthma. Agents administered to treat asthma include bronchodilators, anti-inflammatory agents, leukotriene blockers, and anti-Ige agents. Particular asthma agents include Zafirlukast, Flunisolide, Triamcinolone, Beclomethasone, Terbutaline, Fluticasone, Formoterol, Beclomethasone, Salmeterol, Theophylline, and Xopenex.

Kessler et al. (Eur Respir J (1996) 9:787-794) discusses a link between being overweight or obese and obstructive sleep apnea. Agents administered to treat sleep apnea include Modafinil and amphetamines.

Hepatic disorders and conditions, such as nonalcoholic fatty liver disease, have been linked to being overweight or obese. Tolman et al. (Ther Clin Risk Manag (2007) 6:1153-1163) discusses a link between being overweight or obese and nonalcoholic fatty liver disease. Agents administered to treat nonalcoholic fatty liver disease include antioxidants (e.g., Vitamins E and C), insulin sensitizers (Metformin, Pioglitazone, Rosiglitazone, and Betaine), hepatoprotectants, and lipid-lowering agents.

Skeletal disorders and conditions, such as, back pain and osteoarthritis of weight-bearing joints, have been linked to being overweight or obese. van Saase (J Rheumatol (1988) 15(7):1152-1158) discusses a link between being overweight or obese and osteoarthritis of weight-bearing joints. Agents administered to treat osteoarthritis of weight-bearing joints include Acetaminophen, non-steroidal anti-inflammatory agents (e.g., Ibuprofen, Etodolac, Oxaprozin, Naproxen, Diclofenac, and Nabumetone), COX-2 inhibitors (e.g., Celecoxib), steroids, supplements (e.g. glucosamine and chondroitin sulfate), and artificial joint fluid.

Metabolic disorders and conditions, for example, Prader-Willi Syndrome and polycystic ovary syndrome, have been linked to being overweight or obese. Cassidy (Journal of Medical Genetics (1997) 34:917-923) discusses a link between being overweight or obese and Prader-Willi Syndrome. Agents administered to treat Prader-Willi Syndrome include human growth hormone (HGH), somatropin, and weight loss agents (e.g., Orlistat, Sibutramine, Methamphetamine, Ionamin, Phentermine, Bupropion, Diethylpropion, Phendimetrazine, Benzphetermine, and Topamax).

Hoeger (Obstetrics and Gynecology Clinics of North America (2001) 28(1):85-97) discusses a link between being overweight or obese and polycystic ovary syndrome. Agents administered to treat polycystic ovary syndrome include insulin-sensitizers, combinations of synthetic estrogen and progesterone, Spironolactone, Eflornithine, and Clomiphene. Reproductive disorders and conditions such as sexual dysfunction, erectile dysfunction, infertility, obstetric complications, and fetal abnormalities, have been linked to being overweight or obese. Larsen et al. (Int J Obes (Lond) (2007) 8:1189-1198) discusses a link between being overweight or obese and sexual dysfunction. Chung et al. (Eur Urol (1999) 36(1):68-70) discusses a link between being overweight or obese and erectile dysfunction. Agents administered to treat erectile dysfunction include phosphodiesterase inhibitors (e.g., Tadalafil, Sildenafil citrate, and Vardenafil), prostaglandin E analogs (e.g., Alprostadil), alkaloids (e.g., Yohimbine), and testosterone. Pasquali et al. (Hum Reprod (1997) 1:82-87) discusses a link between being overweight or obese and infertility. Agents administered to treat infertility include Clomiphene, Clomiphene citrate, Bromocriptine, Gonadotropin-releasing Hormone (GnRH), GnRH agonist, GnRH antagonist, Tamoxifen/nolvadex, gonadotropins, Human Chorionic Gonadotropin (HCG), Human Menopausal Gonadotropin (HmG), progesterone, recombinant follicle stimulating hormone (FSH), Urofollitropin, Heparin, Follitropin alfa, and Follitropin beta.

Weiss et al. (American Journal of Obstetrics and Gynecology (2004) 190(4):1091-1097) discusses a link between being overweight or obese and obstetric complications. Agents administered to treat obstetric complications include Bupivacaine hydrochloride, Dinoprostone PGE2, Meperidine HCl, Ferro-folic-500/iberet-folic-500, Meperidine, Methylergonovine maleate, Ropivacaine HCl, Nalbuphine HCl, Oxymorphone HCl, Oxytocin, Dinopro stone, Ritodrine, Scopolamine hydrobromide, Sufentanil citrate, and Oxytocic.

Psychiatric disorders and conditions, for example, weight-associated depression and anxiety, have been linked to being overweight or obese. Dixson et al. (Arch Intern Med (2003) 163:2058-2065) discusses a link between being overweight or obese and depression. Agents administered to treat depression include serotonin reuptake inhibitors (e.g., Fluoxetine, Escitalopram, Citalopram, Paroxetine, Sertraline, and Venlafaxine); tricyclic antidepressants (e.g., Amitriptyline, Amoxapine, Clomipramine, Desipramine, Dosulepin hydrochloride, Doxepin, Imipramine, Iprindole, Lofepramine, Nortriptyline, Opipramol, Protriptyline, and Trimipramine); monoamine oxidase inhibitors (e.g., Isocarboxazid, Moclobemide, Phenelzine, Tranylcypromine, Selegiline, Rasagiline, Nialamide, Iproniazid, Iproclozide, Toloxatone, Linezolid, Dienolide kavapyrone desmethoxyyangonin, and Dextroamphetamine); psycho stimulants (e.g., Amphetamine, Methamphetamine, Methylphenidate, and Arecoline); antipsychotics (e.g., Butyrophenones, Phenothiazines, Thioxanthenes, Clozapine, Olanzapine, Risperidone, Quetiapine, Ziprasidone, Amisulpride, Paliperidone, Symbyax, Tetrabenazine, and Cannabidiol); and mood stabilizers (e.g., Lithium carbonate, Valproic acid, Divalproex sodium, Sodium valproate, Lamotrigine, Carbamazepine, Gabapentin, Oxcarbazepine, and Topiramate).

Simon et al. (Archives of General Psychiatry (2006) 63(7):824-830) discusses a link between being overweight or obese and anxiety. Agents administered to treat anxiety include serotonin reuptake inhibitors, mood stabilizers, benzodiazepines (e.g., Alprazolam, Clonazepam, Diazepam, and Lorazepam), tricyclic antidepressants, monoamine oxidase inhibitors, and beta-blockers.

Another aspect of the invention provides methods for facilitating and maintaining weight loss in a subject involving administering to the subject an amount of a disclosed compound effective to result in weight loss in the subject; and administering a therapeutically effective amount of a different weight loss agent to maintain a reduced weight in the subject. Weight loss agents include serotonin and noradrenergic re-uptake inhibitors; noradrenergic re-uptake inhibitors; selective serotonin re-uptake inhibitors; and intestinal lipase inhibitors. Particular weight loss agents include orlistat, sibutramine, methamphetamine, ionamin, phentermine, bupropion, diethylpropion, phendimetrazine, benzphetermine, bromocriptine, lorcaserin, topiramate, or agents acting to modulate food intake by blocking ghrelin action, inhibiting diacylglycerol acyltransferase 1 (DGAT1) activity, inhibiting stearoyl CoA desaturase 1 (SCD1) activity, inhibiting neuropeptide Y receptor 1 function, activating neuropeptide Y receptor 2 or 4 function, or inhibiting activity of sodium-glucose cotransporters 1 or 2. These compounds are administered in regimens and at dosages known in the art.

EXAMPLES

The compounds described herein can be prepared in a number of ways based on the teachings contained herein and synthetic procedures known in the art. In the description of the synthetic methods described below, it is to be understood that all proposed reaction conditions, including choice of solvent, reaction atmosphere, reaction temperature, duration of the experiment and workup procedures, can be chosen to be the conditions standard for that reaction, unless otherwise indicated. It is understood by one skilled in the art of organic synthesis that the functionality present on various portions of the molecule should be compatible with the reagents and reactions proposed. Substituents not compatible with the reaction conditions will be apparent to one skilled in the art, and alternate methods are therefore indicated. The starting materials for the examples are either commercially available or are readily prepared by standard methods from known materials.

At least some of the compounds identified as “Intermediates” herein are contemplated as compounds of the invention.

¹H NMR spectra were recorded at ambient temperature using a Varian Unity Inova (400 MHz) spectrometer with a triple resonance 5 mm probe for example compounds, and either a Bruker Avance DRX (400 MHz) spectrometer or a Bruker Avance DPX (300 MHz) spectrometer for intermediate compounds. Chemical shifts are expressed in ppm relative to tetramethylsilane. The following abbreviations have been used: br=broad signal, s=singlet, d=doublet, dd=double doublet, ddd=double double doublet, dt=double triplet, t=triplet, td=triple doublet, tt=triple triplet q=quartet, m=multiplet.

Mass Spectrometry (LCMS) experiments to determine retention times and associated mass ions were performed using the following methods:

Method A: Experiments were performed on a Waters Platform LC quadrapole mass spectrometer linked to a Hewlett Packard HP100 LC system with a diode array detector. The spectrometer has an electrospray source operating in positive and negative ion mode. Additional detection was achieved using a Sedex 85 evaporative light scattering detector. LC was carried out using a Phenomenex Luna 3 micron 30×4.6 mm C18 column and a 2 mL/minute flow rate. The initial solvent system was 95% water containing 0.1% formic acid (solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B) for the first 0.5 minute followed by a gradient up to 5% solvent A and 95% solvent B over the next 4 minutes. The final solvent system was held constant for a further 1 minute.

Method B: Experiments were performed on a Waters ZMD LC quadrapole mass spectrometer linked to a Waters 1525 LC system with a diode array detector. The spectrometer has an electrospray source operating in positive and negative ion mode. Additional detection was achieved using a Sedex 85 evaporative light scattering detector. LC was carried out using a Luna 3 micron 30×4.6 mm C18 column and a 2 mL/minute flow rate. The initial solvent system was 95% water containing 0.1% formic acid (solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B) for the first 0.5 minute followed by a gradient up to 5% solvent A and 95% solvent B over the next 4 minutes. The final solvent system was held constant for a further 1 minute.

Method C: Experiments were performed on a Waters Micromass ZQ2000 quadrapole mass spectrometer linked to a Waters Acquity UPLC system with a PDA UV detector. The spectrometer has an electrospray source operating in positive and negative ion mode. LC was carried out using an Acquity BEH 1.7 micron C18 column, an Acquity BEH Shield 1.7 micron RP18 column or an Acquity HSST 1.8 micron column. Each column has dimensions of 100×2.1 mm and was maintained at 40° C. with a flow rate of 0.4 mL/minute. The initial solvent system was 95% water containing 0.1% formic acid (solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B) for the first 0.4 minute followed by a gradient up to 5% solvent A and 95% solvent B over the next 6 minutes. The final solvent system was held constant for a further 0.8 minutes.

Method D: Experiments were performed on a Finnigan AQA single quadrupole mass spectrometer linked to a Hewlett Packard 1050 LC system with a diode array detector. The spectrometer has an electrospray source operating in positive ion mode. Additional detection was achieved using a Sedex 65 evaporative light scattering detector. LC was carried out using a Luna 3 micron 30×4.6 mm C18 column and a 2 mL/minute flow rate. The initial solvent system was 95% water containing 0.1% formic acid (solvent A) and 5% acetonitrile containing 0.1% formic acid (solvent B) for the first 0.5 minute followed by a gradient up to 5% solvent A and 95% solvent B over the next 4 minutes. The final solvent system was held constant for a further 1 minute.

Microwave experiments were carried out using a Biotage Initiator™, which uses a single-mode resonator and dynamic field tuning. Temperatures from 40-250° C. can be achieved, and pressures of up to 20 bars can be reached.

Preparative HPLC purification was carried out using either a C18-reverse-phase column from Genesis (C18) or a C6-phenyl column from Phenomenex (C6 Ph) (100×22.5 mm i.d. with 7 micron particle size, UV detection at 230 or 254 nm, flow 5-15 mL/min), eluting with gradients from 100-0 to 0-100% water/acetonitrile or water/methanol containing 0.1% formic acid. Fractions containing the required product (identified by LCMS analysis) were pooled, the organic fraction removed by evaporation, and the remaining aqueous fraction lyophilised, to give the product.

Chiral HPLC was carried out using a Chiralpak IC column, 4.4 mm×250 mm, particle size 5 micron

Compounds which required column chromatography were purified manually or fully automatically using either a Biotage SP1™ Flash Purification system with Touch Logic Control™ or a Combiflash Companion® with pre-packed silica gel Isolute® SPE cartridge, Biotage SNAP cartridge or Rcdiscp® Rf cartridge respectively.

Compounds have been named using Autonom2000 in ISISDraw

Abbreviations:

-   DCM Dichloromethane -   DMF N,N-Dimethylformamide -   DMAP 4-dimethylaminopyridine -   DMA N,N-Dimethylacetamide -   AIBN Azo-bis-(isobutyronitrile) -   THF Tetrahydrofuran. -   DMAW 350 DCM, methanol, acetic acid, water (350:20:3:2) -   DMAW 240 DCM, methanol, acetic acid, water (240:20:3:2) -   DMAW 120 DCM, methanol, acetic acid, water (120:15:3:2) -   TFA Trifluoroacetic acid

Example 1 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid

Methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 4, 0.129 g) was added to a solution of lithium hydroxide monohydrate (0.42 g) in water (2 mL) and dioxane (8 mL), and the mixture was sealed in a microwave vial and heated at 130° C. for 1 hour in the microwave. After cooling, the mixture was acidified with formic acid, and evaporated to dryness. The residue was triturated with 10% methanol in DCM, filtered and the filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM with a gradient of 0-10%. The product was triturated with ethyl acetate, filtered and dried in vacuo to give 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid (0.056 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.71 (1H, d), 7.68 (1H, d), 7.38 (1H, d), 7.28 (1H, dd), 7.26-7.19 (2H, m), 7.02 (1H, d), 6.86 (1H, d), 6.20-6.11 (1H, m), 5.28 (2H, s), 3.79 (2H, d), 3.12 (4H, q), 1.14 (6H, t).

LCMS (Method C) r/t 3.48 (M+H) 501

Example 2 7-(Benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 1, starting from methyl 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 11)

¹H NMR (DMSO-d₆) δ: 7.76 (1H, dd), 7.74-7.72 (3H, m), 7.62 (2H, dd), 7.35 (1H, d), 6.94 (1H, d), 6.69 (1H, d), 5.45 (2H, s), 4.71 (2H, s).

LCMS (Method C) r/t 3.93 (M+H) 371

Example 3 8-(Benzenesulfonylmethyl)-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid

Prepared by proceeding in a similar manner to Example 1, starting from methyl 8-benzenesulfonylmethyl-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate (Intermediate 12).

¹H NMR (CD₃OD) δ: 7.73 (2H, m), 7.67 (1H, m), 7.58 (1H, d), 7.56-7.51 (2H, m), 7.47 (1H, d), 6.94 (1H, d), 6.81 (1H, d), 4.64 (2H, s), 4.25 (2H, t), 3.22 (2H, t).

LCMS (Method C) r/t 4.06 (M+Na) 407

Example 4 7-(Benzenesulfonylmethyl)-furo[2,3-c]quinoline-6-carboxylic acid

Trifluoroacctic acid (2 mL) was added to a solution of tert-butyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-(2-hydroxyacetylamino)-6-benzoate (Intermediate 31, 0.17 g) in DCM (8 mL) and the resultant mixture was stirred for 18 hours. The mixture was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM with a gradient of 3-5%. The product was repurified by HPLC (C18) eluting with a mixture of methanol and water containing 0.1% formic acid, with a gradient of 50-60% to give methyl 7-(benzenesulfonylmethyl)-furo[2,3-c]quinoline-6-carboxylate (0.012 g) as a white solid.

¹H NMR (CDCl₃) δ: 9.13 (1H, d), 8.38 (1H, d), 8.11 (1H, d), 8.02 (1H, d), 7.79 (2H, dd), 7.59 (1H, t), 7.45-7.44 (3H, m), 5.74 (2H, s).

LCMS (Method C) r/t 3.45 (M+H) 368

Example 5 7-(Benzenesulfonylmethyl)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 4, starting from tert-butyl 7-(benzenesulfonylmethyl)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 13)

¹H NMR (DMSO-d₆) δ: 13.77 (1H, br, s), 8.43 (1H, d), 8.05 (1H, d), 7.76-7.69 (3H, m), 7.62 (2H, t), 7.52 (1H, d), 7.20 (1H, d), 4.92 (2H, s).

LCMS (Method C) r/t 3.45 (M+Na) 407.

Example 6 7-(Benzenesulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 1, starting from methyl 7-(benzenesulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 14).

¹H NMR (DMSO-d₆) δ: 7.76 (1H, m), 7.73 (3H, d), 7.62 (2H, dd), 7.37 (1H, d), 6.95 (1H, d), 6.72 (1H, d), 5.74-5.67 (1H, m), 4.71 (2H, s), 1.53 (3H, d).

LCMS (Method C) r/t 4.19 (M+Na) 407

Example 7 8-[2((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid

Prepared by proceeding in a similar manner to Example 1, starting from methyl 8-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate (Intermediate 5).

¹H NMR (DMSO-d₆) δ: 7.72 (1H, dd), 7.62 (1H, d), 7.51 (1H, d), 7.38 (1H, d), 7.25 (2H, m), 7.15 (1H, d), 6.88 (1H, d), 6.22-6.13 (1H, m), 4.05 (2H, t), 3.81 (2H, d), 3.24 (2H, br, s), 3.13 (4H, t), 1.14 (6H, t).

LCMS (Method C) r/t 3.52 (M+H) 515

Example 8 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid

Lithium hydroxide monohydrate (0.107 g) was added to a solution of methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]-quinoline-6-carboxylate (Intermediate 6, 0.026 g) in a mixture of dioxane (1.7 mL) and water (0.8 mL). The resultant mixture was stirred and heated at 90° C. overnight. After cooling, the mixture was acidified by addition of formic acid and then evaporated to dryness. The residue was triturated with a mixture of methanol and DCM (10%) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM with a gradient of 0-12%. The product was triturated with a mixture of DCM and diethyl ether (50%) and the solid was collected by filtration and dried in vacuo to give 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid (0.013 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 13.11 (1H, br, s), 9.07 (1H, s), 8.15-8.12 (4H, m), 7.35-7.26 (2H, m), 7.12 (1H, m), 6.92 (1H, dd), 6.17 (1H, dt), 3.61 (2H, d), 2.96 (4H, q), 1.20 (6H, t).

LCMS (Method C) r/t 2.89 (M+H) 498

Example 9 7-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid

A mixture of methyl 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 45, 0.130 g) and lithium hydroxide (0.105 g) in dioxane (3 mL) and water (1 mL) was heated at 90° C. for 20 hours. After cooling, the mixture was diluted with water (20 mL) and acidified to pH5-6 with formic acid. This was extracted into ethyl acetate. The combined organic layers were dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-10%. The product was triturated with diethyl ether/ethyl acetate (1:1) to give 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid (0.025 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.95 (1H, dd), 7.48 (1H, d), 7.21-7.13 (3H, m), 7.03 (1H, td), 6.68 (1H, d), 5.29 (2H, s), 3.25 (6H, m), 3.13 (2H, m), 2.08-1.98 (2H, m), 1.34 (6H, t).

LCMS (Method C) r/t 3.51 (M+H) 503

Example 10 7-[2((Z)-3-Ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid

A mixture of methyl 7-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 46, 0.096 g) and lithium hydroxide monohydrate (0.168 g) in water (0.8 mL) and dioxane (3.2 mL), was sealed in a microwave vial and irradiated in the microwave at 135° C. for 45 minutes. After cooling, the mixture was diluted with ethanol, acidified with formic acid and evaporated to dryness. The residue was triturated with 10% methanol in DCM, filtered and the filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with DMAW 350. The product was azeotroped with toluene and ethanol and the residue was triturated with ethyl acetate to give 7-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid (0.020 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.71 (1H, d), 7.60 (1H, dd), 7.31-7.10 (5H, m), 6.87 (1H, d), 6.00 (1H, dt), 5.27 (2H, s), 3.68 (2H, d), 3.00 (2H, q), 1.18 (3H, t).

LCMS (Method C) r/t 3.53 (M+H) 473

Example 11 8-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid

A mixture of methyl 8-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate (Intermediate 50, 0.134 g) and lithium hydroxide monohydrate (0.159 g) in water (3.8 mL) and dioxane (3.8 mL) was sealed in a microwave vial and irradiated in the microwave at 130° C. for 30 minutes. The mixture was concentrated in vacuo, water was added and it was acidified to pH3 with formic acid. This was extracted into ethyl acetate, dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 2.5-10%. The resultant product was recrystallised from a mixture of DCM and ethyl acetate to give 8-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid (0.036 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.97-7.91 (1H, m), 7.54 (1H, d), 7.41 (1H, d), 7.34 (1H, d), 6.90-6.89 (2H, m), 6.62 (1H, d), 4.26 (2H, t), 3.21 (10H, m), 2.08-1.98 (2H, m), 1.38 (6H, t).

LCMS (Method C) r/t 3.55 (M+H) 517

Example 12 7-{4-Fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid

A mixture of methyl 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 51, 0.408 g) and lithium hydroxide monohydrate (0.526 g) in water (2.5 mL) and dioxane (10 mL), was sealed in a microwave vial and irradiated in the microwave at 135° C. for 45 minutes. After cooling, the mixture was diluted with ethanol, acidified with formic acid and evaporated to dryness. The residue was triturated with 10% methanol in DCM and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with DMAW 350. The resultant product was azeotroped with toluene and ethanol to give a solid which was triturated with methanol. The solid was collected by filtration and purified by chromatography on silica, eluting with methanol and DCM, with a gradient of 0-10%. The resultant product was triturated with acetone the solid was collected by filtration to give 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid (0.155 g) as a white solid.

¹H NMR (DMSO-d₆) δ 7.72 (1H, d), 7.63 (1H, dd), 7.35-7.22 (4H, m), 6.97 (1H, d), 6.88 (1H, d), 6.20-6.12 (1H, m), 5.31 (2H, s), 3.72 (4H, br, t), 3.64 (2H, d), 3.05 (4H, br, s).

LCMS (Method C) r/t 3.54 (M+H) 515

Example 13 7-{4-Fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 9, starting from methyl 7-{4-fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 53).

¹H NMR (CD₃OD) δ: 7.74 (1H, dd), 7.56 (1H, d), 7.51 (1H, d), 7.23 (2H, d), 7.13-7.04 (2H, m), 6.73 (1H, d), 6.19-6.10 (1H, m), 5.28 (2H, s), 3.99 (2H, d), 3.25 (4H, m), 2.07 (4H, br, s).

LCMS (Method C) r/t 3.56 (M+H) 499

Example 14 7-[2((Z)-(3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid

tert-Butyl 7-[2((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 55, 0.185 g) was suspended in DCM (3 mL) and TFA (3 mL) was added. The reaction mixture was stirred at room temperature for 3 hours. The mixture was concentrated in vacuo and the residue was dissolved in methanol. Potassium carbonate (0.100 g) was added and the resultant mixture was stirred for a few minutes. The inorganic salts were removed by filtration and the filtrate was acidified to pH 3 with formic acid. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 2.5-10%. The resultant product was triturated with ethyl acetate, dried in vacuo at 60° C. to give 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid (0.070 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.96 (1H, d), 7.71 (2H, d), 7.67-7.60 (2H, m), 7.10 (1H, d), 6.94 (2H, d), 6.20-6.10 (1H, m), 3.92 (2H, d), 3.32 (4H, br, q), 1.38 (6H, t).

LCMS (Method C) r/t 3.31 (M+H) 515

Example 15 7-[2((Z)-(3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid

A mixture of methyl 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 64, 0.070 g) and lithium hydroxide monohydrate (0.200 g) in dioxane (3 mL) and water (1 mL) was heated at 80° C. for 3 hours. The resultant mixture was cooled, neutralised by addition of saturated aqueous ammonium chloride solution and concentrated in vacuo. The residue was extracted with DCM, dried (MgSO₄) and filtered. The filtrate was concentrated and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-15%. The resultant product was triturated with diethyl ether and the solid obtained was dried in vacuo to give 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid (0.025 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 7.71 (1H, dd), 7.51 (1H, m), 7.44 (1H, d), 7.29-7.21 (3H, m), 7.02 (1H, d), 6.89 (1H, d), 6.29 (1H, m), 5.45-5.44 (1H, m), 4.72 (2H, q), 3.91 (2H, br, d), 3.08 (4H, br, q), 1.40 (3H, d), 1.16 (6H, t).

LCMS (Method C) r/t 3.32 (M+H) 514

Example 16 7-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid

A mixture of methyl 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylate (Intermediate 71, 0.100 g) and lithium hydroxide monohydrate (0.250 g) in dioxane (4 mL) and water (1.25 mL) was heated at 80° C. overnight. The mixture was cooled and saturated aqueous ammonium chloride was added. This was concentrated in vacuo and the residue was triturated with DCM and methanol, filtered and the filtrate was concentrated in vacuo. The residue was purified by HPLC (C6 Ph) eluting with a mixture of methanol and water containing 0.1% formic acid, with a gradient of 10-40% to give a yellow gum. The product was triturated with ether to give 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-furo[2,3-c]quinoline-6-carboxylic acid (0.045 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 9.06 (1H, d), 8.33 (1H, br, s), 8.20 (1H, d), 8.15-8.05 (3H, m), 7.32 (1H, dd), 7.10 (1H, dd), 6.97 (1H, ddd), 3.13-3.02 (8H, m), 2.17-2.06 (2H, m), 1.30 (6H, t).

LCMS (Method C) r/t 2.97 (M+H) 500

Example 17 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-chromeno[3,4-d]isothiazole-6-carboxylic acid

Methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-chromeno[3,4-d]isothiazole-6-carboxylate (Intermediate 72, 0.058 g) was dissolved in dioxane (1.5 mL) and water (0.6 mL). Lithium hydroxide monohydrate (0.018 g) was added and the resultant mixture was heated at 85° C., under nitrogen for 3 hours. The mixture was left to cool overnight. A further amount of lithium hydroxide monohydrate (0.010 g) was added and the mixture was heated at 85° C. for a further 1 hour. The mixture was cooled, diluted with DCM and acidified to pH4 with aqueous formic acid (10%), to give an emulsion. The emulsion was concentrated in vacuo to give a gum, which was triturated with a solution of 2M methanol in DCM and the solid was removed by filtration. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-8%. The resultant product was dissolved in acetonitrile and water and freeze-dried overnight to give 7-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-chromeno[3,4-d]isothiazole-6-carboxylic acid (0.027 g) as a white solid.

¹H NMR (DMSO-d₆) δ: 8.38 (1H, s), 7.90 (1H, dd), 7.40-7.26 (3H, m), 7.21 (1H, dd), 6.98 (1H, d), 6.08-5.99 (1H, m), 5.29 (2H, s), 3.76 (2H, br, d), 3.03 (4H, br, q), 1.05 (6H, t).

LCMS (Method C) r/t 3.26 (M+H) 518

Example 18 Separation of Enantiomers of 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid

Sample from Example 15 was subjected to chiral separation eluting with isopropanol and heptane (1:1) to give two products:

Example 18A First Eluting Enantiomer, r/t 22.67 Minutes (ee 98%)

¹H NMR (DMSO-d₆) δ: 7.72 (1H, dd), 7.53 (1H, m), 7.45 (1H, d), 7.26 (3H, m), 7.03 (1H, d), 6.90 (1H, d), 6.31-6.29 (1H, m), 5.49-5.42 (1H, m), 4.74-4.72 (2H, q), 4.01-3.84 (2H, m), 3.09 (4H, q), 1.41 (3H, d), 1.17 (6H, t).

LCMS (Method C) r/t 3.33 (M+H) 514

Example 18B Second Eluting Enantiomer r/t 29.36 Minutes (ee 85%)

¹H NMR (DMSO-d₆) δ: 7.72 (1H, dd), 7.53 (1H, m), 7.45 (1H, d), 7.26 (3H, m), 7.03 (1H, d), 6.90 (1H, d), 6.31-6.29 (1H, m), 5.49-5.42 (1H, q), 4.74-4.72 (2H, q), 4.01-3.84 (2H, m), 3.09 (4H, q), 1.41 (3H, d), 1.17 (6H, t).

LCMS (Method C) r/t 3.30 (M+H) 514

Example 19 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-benzenesulfonylamino-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 11, starting from methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-benzenesulfonylamino-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 80).

¹H NMR (DMSO-d₆) δ: 7.69 (2H, m), 7.60 (1H, t), 7.46-7.37 (2H, m), 7.30 (1H, d), 7.22 (1H, d), 7.03 (1H, d), 6.85 (1H, d), 6.15-6.06 (1H, m), 5.26 (2H, s), 3.74 (2H, br, s), 3.09 (4H, br, s), 1.12 (6H, t).

LCMS (Method C) r/t 3.35 (M+H) 483

Example 20 7-{4-Fluoro-2-[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid

A mixture of methyl 7-{4-fluoro-2-[(Z)-3-((R)-3-acetoxypyrrolidin-1-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 82, 0.092 g) and lithium hydroxide monohydrate (0.039 g) in water (2 mL) and dioxane (4 mL), was scaled in a microwave vial and irradiated in the microwave at 110° C. for 20 minutes. After cooling, the mixture was diluted with water (20 mL), acidified with formic acid to pH 4-5 and extracted into DCM. The organic layer was dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by HPLC (C6 Ph) eluting with a mixture of acetonitrile and water, containing 0.1% formic acid, with a gradient of 30-60%, to give 7-{4-fluoro-2-[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid (0.004 g).

¹H NMR (CD₃OD) δ: 8.55 (1H, s), 7.79 (1H, m), 7.51 (2H, m), 7.24-7.15 (2H, m), 7.14-7.06 (2H, m), 6.72 (1H, d), 6.14 (1H, m), 5.29 (2H, s), 4.54 (1H, m), 3.95 (2H, br, m), 3.6 (3H, br), 3.4 (1H, br), 2.19 (1H, br, m), 2.00 (1H, br, m).

LCMS (Method C) r/t 3.39 (M+H) 515

Example 21 7-{4-Fluoro-2-[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 20, starting from methyl 7-{4-fluoro-2-[(Z)-3-((S)-3-acetoxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 84).

¹H NMR (CD₃OD) δ: 8.29 (1H, br, s), 7.73 (1H, dd), 7.56 (1H, br, d), 7.50 (1H, m), 7.22 (2H, s), 7.08 (1H, s), 7.06 (1H, s), 6.72 (1H, d), 6.15 (1H, dt), 5.27 (2H, s), 4.54 (2H, m), 4.15-3.98 (2H, m), 3.66-3.22 (3H, br), 2.20 (1H, m), 2.03 (1H, m).

LCMS (Method C) r/t 3.40 (M+H) 515

Example 22 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylic acid

A mixture of 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylic acid (Intermediate 86, 0.190 g), N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3, 0.476 g), tris-(dibenzylideneacetone)dipalladium (0.043 g) and tri-tert-butylphosphonium tetrafluoroborate (0.023 g) in dioxane (5 mL) was heated under argon to 80° C. in a sealed vessel for 1 hour. The hot reaction mixture was filtered through Celite and washed with dioxane, ethyl acetate and acetonitrile. The filtrate was concentrated in vacuo and the residue was triturated with water and acetonitrile and then acetone. The solid was collected by filtration, dissolved in DMSO and filtered. The filtrate was purified by HPLC (C18) eluting with a mixture of acetonitrile and water, containing 0.1% formic acid, with a gradient of 25-75% acetonitrile, to give 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylic acid (0.062 g).

¹H NMR (DMSO-d₆) δ: 14.43 (1H, s), 8.17-8.10 (2H, m), 7.89 (1H, d), 7.38-7.32 (3H, m), 7.22-7.21 (2H, m), 5.95 (1H, m), 3.74 (2H, br, s), 2.92 (4H, br, s), 0.93 (6H, t).

LCMS (Method C) r/t 3.41 (M+H) 514

Example 23 7-{2-[(Z)-3-(Azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonyl-amino}-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 20, starting from methyl 7-{2-[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 91).

¹H NMR (CD₃OD) δ: 7.74 (1H, dd), 7.54-7.49 (2H, m), 7.26 (2H, m), 7.12-6.99 (2H, m), 6.73 (1H, d), 5.99-5.89 (1H, dt), 5.29 (2H, s), 4.57 (1H, br, s), 4.29 (2H, br, s), 4.12 (2H, br, s), 3.98 (2H, dd), 2.64-2.35 (2H, br, m).

LCMS (Method C) r/t 3.53 (M+H) 485

Example 24 7-{4-Fluoro-2-[(Z)-3-(3-hydroxyazetidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 20, starting from methyl 7-{4-fluoro-2-[(Z)-3-(3-acetoxyazetidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 94).

¹H NMR (CD₃OD) δ: 7.73 (1H, dd), 7.55-7.51 (2H, m), 7.30-7.21 (2H, m), 7.12-7.00 (2H, m), 6.73 (1H, d), 6.02-5.92 (1H, m), 5.29 (2H, s), 4.66 (1H, m), 4.47 (2H, br, m), 4.03 (2H, d), 3.92 (2H, br, m).

LCMS (Method C) r/t 3.45 (M+H) 501

Example 25 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylic acid

Prepared by proceeding in a similar manner to Example 12, starting from methyl 7-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 96).

¹H NMR (DMSO-d₆) δ: 7.97 (1H, d), 7.73 (1H, dd), 7.38 (1H, d), 7.32-7.16 (3H, m), 7.07 (1H, d), 6.18-6.09 (1H, m), 5.21 (2H, s), 3.79 (2H, br, d), 3.11 (4H, br, q), 1.13 (6H, t).

LCMS (Method C) r/t 3.67 (M+H) 519

Example 26 7-[2-((E)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid

A mixture of methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 4, 1.73 g) and lithium hydroxide monohydrate (1.41 g) in dioxane (27 mL) and water (9 mL) was heated to 100° C. for 16 hours, under an atmosphere of nitrogen. The mixture was cooled to room temperature and diluted with DCM (100 mL) and water (100 mL). This mixture was acidified to pH6 using formic acid and the layers were separated. The aqueous layer was extracted with a further 3×100 mL DCM. The combined organic layers were washed with brine, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo to give a tan solid. This was purified by chromatography on silica, eluting with a mixture of 2M ammonia solution in methanol and DCM with a gradient of 10-20% to give 7-[2-((E)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylic acid (0.133 g), isolated as the minor by-product of the reaction.

¹H NMR (DMSO-d₆) δ 7.98 (1H, dd), 7.67 (1H, d), 7.63 (1H, dd), 7.47 (1H, d), 7.26 (1H, td), 7.16 (1H, d), 7.05 (1H, d), 6.80 (1H, d), 6.71-6.61 (1H, m), 5.28 (2H, s), 3.82 (2H, d), 3.21 (4H, m), 1.29 (6H, t).

LCMS (Method C) r/t 3.63 (M+H) 501

Intermediate 1 (Z)-3-Tributylstannanylprop-2-en-1-ol

Propargyl alcohol (5 mL) was added to a solution of lithium aluminium hydride (1M in THF, 43 mL) in THF (70 mL) at −78° C. The resultant mixture was warmed to room temperature and stirred for 18 hours. It was re-cooled to −78° and a solution of tri-n-butyl tin chloride (8.32 mL) in diethyl ether (50 mL) was added and the mixture was stirred for 3 hours whilst gradually warming to room temperature. The reaction mixture was cooled to −5° C. and quenched by addition of water and 15% aqueous sodium hydroxide solution then warmed to room temperature. Ethyl acetate was added and the mixture was stirred for 1 hour. The precipitate was filtered through Celite and the filtrate was evaporated to dryness. The residue was purified by chromatography on a silica column which had been pre-washed with 20% triethylamine in acetonitrile. The column was eluted with a mixture of ethyl acetate and pentane with a gradient of 0-10% to give (Z)-3-tributylstannanyl-prop-2-en-1-ol (5.06 g) as a clear oil.

¹H NMR (CDCl₃) δ: 6.70 (1H, dt), 6.08 (1H, dt), 4.12 (2H, dd), 1.49 (6H, m), 1.31 (6H, m), 0.98-0.84 (15H, m).

Intermediate 2 ((Z)-3-Bromoprop-1-enyl)-tributylstannane

A solution of triphenylphosphine (5.32 g) in DCM (60 mL) was added to a solution of (Z)-3-tributylstannanylprop-2-en-1-ol (Intermediate 1, 6.4 g) and carbon tetrabromide (9.18 g) in DCM (60 mL) and the mixture was stirred for 2.5 hours. The mixture was evaporated to low volume and pentane was added. The solids were removed by filtration and the filtrate was evaporated to dryness. Pentane was added and the solids were again removed by filtration and the filtrate was evaporated to dryness to give ((Z)-3-bromoprop-1-en-1-yl)-tributylstannane (12.14 g) as an oil.

¹H NMR (CDCl₃) δ: 6.71 (1H, dt), 6.11 (1H, d), 3.88 (2H, d), 1.52-1.50 (6H, m), 1.37-1.27 (6H, m), 0.99-0.97 (6H, m), 0.90 (9H, t).

Intermediate 3 N,N-Diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine

Diethylamine (19 mL) was added to a solution of ((Z)-3-bromoprop-1-enyl)-tributyl-stannane (Intermediate 2, 7.52 g) in THF (60 mL) and the mixture was stirred for 3 hours. The reaction mixture was evaporated to dryness and the residue was purified by chromatography on a silica column which had been pre-washed with 20% triethylamine in acetonitrile. The column was eluted with a mixture of ethyl acetate and pentane with a gradient of 0-10% to give N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (4.75 g) as an orange oil.

¹H NMR (CDCl₃) δ: 6.59 (1H, dt), 5.97 (1H, dt), 3.08 (2H, dd), 2.53 (4H, q), 1.49 (6H, m), 1.37-1.24 (6H, m), 1.04 (6H, t), 0.92-0.89 (15H, m).

Intermediate 4 Methyl 7-[2((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate

A mixture of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 7, 0.378 g), N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)amine (Intermediate 3, 0.41 g), tri-tert-butylphosphinium tetrafluoroborate (0.023 g), tris-(dibenzylideneacetone)dipalladium (0.036 g) in dioxane (6 mL) and DMSO (0.6 mL) was sealed in a microwave vial, under nitrogen and heated at 150° C. in the microwave for 45 minutes. After cooling, the mixture was diluted with ethyl acetate and water, the organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM with a gradient of 0-10% to give methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (0.13 g) as a brown foam. This material was used without further characterisation.

Intermediate 5 Methyl 8-[2[((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate

Prepared by proceeding in a similar manner to Intermediate 4, starting from methyl 8-(2-bromo-4-fluorobenzenesulfonylamino)-4,5-dihydro-3,6-dioxa-benzo[e]azulene-7-carboxylate (Intermediate 8) and N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3).

¹H NMR (CDCl₃) δ: 8.10 (1H, dd), 7.48 (1H, d), 7.37 (1H, d), 7.14 (1H, m), 7.09 (1H, d), 7.01 (2H, m), 6.59 (1H, d), 6.18 (1H, m), 4.26 (2H, t), 3.90 (3H, s), 3.30 (2H, br, s), 3.24 (2H, t), 2.69-2.61 (4H, m), 1.04 (6H, m).

Intermediate 6 Methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylate

A mixture of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-furo[2,3-c]quinoline-6-carboxylate (Intermediate 9, 0.165 g), N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3, 0.3 g), tri-tert-butylphosphinium tetrafluoroborate (0.01 g), tris-(dibenzylideneacetone)dipalladium (0.019 g) in dioxane (6 mL) was degassed then heated at 100° C. for 75 minutes. After cooling, the mixture was evaporated to approximately half volume then partitioned between ethyl acetate and water. The organic layer was washed with water, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-14% to give methyl 7-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylate (0.028 g) as a yellow solid.

¹H NMR (DMSO-d₆) δ: 9.01 (1H, s), 8.22 (1H, d), 8.01 (1H, dd), 7.93 (1H, m), 7.64 (1H, d), 7.58-7.53 (1H, m), 7.46 (1H, s), 7.19 (1H, m), 7.08-7.03 (1H, m), 6.87 (1H, s), 3.80 (3H, s), 2.90-2.82 (2H, m), 1.36 (4H, m), 0.90 (6H, t).

Intermediate 7 Methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate

Methyl 7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate (Intermediate 10, 0.73 g) was stirred in 4M HCl in dioxane (10 mL) for 1.5 hours. The mixture was evaporated to dryness and the crude residue was dissolved in DCM (5 mL) and pyridine (5 mL) and treated with 2-bromo-4-fluorobenzenesulfonyl chloride (0.49 g). The resultant mixture was stirred for 18 hours then evaporated to dryness. The residue was dissolved in ethyl acetate and acidified with 1M HCl. The organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of DCM and cyclohexane with a gradient of 50-75%. The isolated fractions were repurified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 10-30% to give methyl 7-(2-bromo-4-fluoro-benzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (0.47 g) as a white solid.

¹H NMR (CDCl₃) δ: 9.27 (1H, br, s), 8.16 (1H, dd), 7.44 (1H, dd), 7.41 (1H, m), 7.16 (2H, d), 7.12 (1H, m), 6.56 (1H, d), 5.38 (2H, s), 3.94 (3H, s).

Intermediate 8 Methyl 8-(2-bromo-4-fluorobenzenesulfonylamino)-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate

2-Bromo-4-fluorobenzenesulfonyl chloride (0.55 g) was added to a solution of methyl 8-amino-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate (Intermediate 15, 0.47 g) and pyridine (3 mL) in DCM (5 mL) and the mixture was stirred for 18 hours. The mixture was evaporated to dryness and water and ethyl acetate were added. The organic layer was separated, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 5-25% to give methyl 8-(2-bromo-4-fluorobenzenesulfonylamino)-4,5-dihydro-3,6-dioxa-benzo[e]azulene-7-carboxylate (0.86 g) as a white solid.

¹H NMR (CDCl₃) δ: 9.03 (1H, br, s), 8.17 (1H, dd), 7.48 (1H, d), 7.43 (1H, dd), 7.36 (1H, d), 7.28 (1H, m), 7.12 (1H, m), 6.59 (1H, d), 4.26 (2H, t), 3.95 (3H, s), 3.24 (2H, t).

Intermediate 9 Methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-furo[2,3-c]quinoline-6-carboxylate

A solution of 2-bromo-4-fluorobenzenesulfonyl chloride (0.57 g) in pyridine (10 mL) was heated to 70° C. and a solution of methyl 7-amino-furo[2,3-c]quinoline-6-carboxylate (Intermediate 16, 0.33 g) in pyridine (10 mL) was added. The mixture was stirred and heated at 70° C. for 4 hours. Further 2-bromo-4-fluorobenzenesulfonyl chloride (0.57 g) was added and the mixture was stirred and heated at 70° C. overnight. After cooling, the mixture was filtered and the solid was washed with methanol. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 15-60%. The product was triturated with diethyl ether and the solid was collected by filtration to give methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-furo[2,3-c]quinoline-6-carboxylate (0.16 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 9.16 (1H, s), 8.60 (1H, br, s), 8.11 (2H, m), 7.96 (1H, d), 7.90 (1H, m), 7.44 (1H, dd), 7.23 (1H, m), 7.06 (1H, m), 4.07 (3H, s).

Intermediate 10 Methyl 7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate

Carbon tetrabromide (2.66 g) was added to a solution of methyl 6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)-benzoate (Intermediate 17, 2.65 g) and triphenyl phosphine (2.1 g) in DCM (40 mL) and the resultant solution was stirred at room temperature for 1 hour. The mixture was evaporated to dryness and DMF (60 mL) and cesium carbonate (5.59 g) were added to the residue. The resultant mixture was stirred for 1 hour, then partitioned between ethyl acetate and water. The organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 5-25% to give methyl 7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate (0.735 g) as a gum which crystallised on standing.

¹H NMR (CDCl₃) δ: 7.45 (1H, m), 7.26 (1H, s), 6.79 (1H, d), 6.65 (1H, d), 5.44 (2H, s), 3.87 (3H, s), 1.42 (18H, s).

Intermediate 11 Methyl 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-benzoate

Carbon tetrabromide (0.116 g) was added to a solution of methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)-benzoate (Intermediate 19, 0.1 g) and triphenyl phosphine (0.09 g) in DCM (3 mL) and the resultant solution was stirred at room temperature for 2 hours. The mixture was evaporated to dryness and the residue was dissolved in DMF (2 mL) and cesium carbonate (0.163 g) was added. The mixture was stirred for 1 hour at room temperature, then at 50° C. for 15 minutes. After cooling, the mixture was partitioned between ethyl acetate and water, the organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane (25%) to give methyl 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylate (0.019 g).

¹H NMR (CDCl₃) δ: 7.71 (2H, dd), 7.64-7.59 (1H, m), 7.50-7.45 (2H, m), 7.43-7.43 (1H, m), 7.18 (1H, d), 6.78 (1H, d), 6.62 (1H, d), 5.38 (2H, s), 4.53 (2H, s), 3.82 (3H, s).

Intermediate 12 Methyl 8-(benzenesulfonylmethyl)-4,5-dihydro-3,6-dioxa-benzo[e]azulene-7-carboxylate

Prepared by proceeding in a similar manner to Intermediate 10, starting from methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-[2-(2-hydroxyethyl)-furan-3-yl]-benzoate (Intermediate 23).

¹H NMR (CDCl₃) δ: 7.70 (2H, d), 7.61 (1H, d), 7.49 (3H, m), 7.40 (1H, s), 7.01 (1H, d), 6.68 (1H, d), 4.52 (2H, s), 4.27 (2H, t), 3.82 (3H, s), 3.26 (2H, t).

Intermediate 13 tert-Butyl 7-(benzenesulfonylmethyl)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate

N,N′-dicyclohexylcarbodiimide (0.014 g) was added to a solution of 3-[4-(benzenesulfonylmethyl)-3-tert-butoxycarbonyl-2-hydroxyphenyl]-furan-2-carboxylic acid (Intermediate 21, 0.028 g) and DMAP (0.0003 g) in DCM (5 mL) and the mixture was stirred for 72 hours. Water and DCM were added and the organic layer was separated, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 30-40% to give tert-butyl 7-(benzenesulfonylmethyl)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (0.037 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.92 (1H, d), 7.80-7.76 (2H, m), 7.71 (1H, s), 7.65 (1H, d), 7.52 (2H, t), 7.36 (1H, d), 7.03 (1H, d), 4.67 (2H, s), 1.67 (9H, s).

Intermediate 14 Methyl 7-(benzenesulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylate

Diisopropyl azodicarboxylate (0.02 g) was added to a solution of methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-[2-(1-hydroxyethyl)-furan-3-yl]-benzoate (Intermediate 20, 0.042 g) and triphenylphosphine (0.026 g) in THF (2 mL) and the mixture was stirred for 1 hour. The mixture was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 5-10% to give methyl 7-(benzenesulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylate (0.038 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.71 (2H, d), 7.61 (1H, t), 7.48 (2H, t), 7.41 (1H, d), 7.18 (1H, d), 6.79 (1H, d), 6.61 (1H, d), 5.59 (1H, q), 4.53 (2H, s), 3.82 (3H, s), 1.61 (3H, d).

Intermediate 15 Methyl 8-amino-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate

Prepared by proceeding in a similar manner to Intermediate 14 starting from methyl 6-amino-2-hydroxy-3-[2-(2-hydroxyethyl)-furan-3-yl]-benzoate (Intermediate 25).

LCMS (Method D) r/t 3.23 (M+H) 260.

Intermediate 16 Methyl 7-aminofuro[2,3-c]quinoline-6-carboxylate

1M Hydrochloric acid (14 drops) was added to a solution of iron (II) sulfate heptahydrate (18.44 g) in water (50 mL) and the resultant solution was added to methyl 6-amino-3-(2-formylfuran-3-yl)-2-nitrobenzoate (Intermediate 30, 2.02 g). The resultant mixture was stirred and heated at reflux for 10 minutes then cooled to 70° C. Methanol (50 mL) was added followed by aqueous ammonia (33%, 19.2 mL) and the mixture was stirred and heated at reflux for 5 hours. After cooling, methanol (50 mL) was added and the mixture was filtered through Celite and the filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with a DMAW 350 followed by DMAW 240 and DMAW 120 to give methyl 7-aminofuro[2,3-c]quinoline-6-carboxylate (0.27 g) as a brown solid.

¹H NMR (DMSO-d₆) δ: 9.08 (1H, s), 8.33-8.31 (1H, m), 8.15 (1H, d), 7.56 (1H, m), 7.26-7.17 (1H, m), 6.09 (2H, br, s), 3.89 (3H, s).

Intermediate 17 Methyl 6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)-benzoate

1M aqueous sodium hydroxide (50 mL) was added to a solution of methyl 6-[bis-(tert-butoxycarbonyl)amino]-3-(2-hydroxymethylfuran-3-yl)-2-(4-methylbenzene-sulfonyloxy)-benzoate (Intermediate 18, 3.82 g) in methanol (100 mL) and the mixture was stirred and heated at 45° C. for 1.5 hours. The mixture was evaporated to dryness and the residue was dissolved in ethyl acetate and acidified with acetic acid. The organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 10-50% to give methyl 6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)-benzoate (2.65 g) as a white foam.

¹H NMR (CDCl₃) δ: 11.91 (1H, s), 7.50 (2H, m), 6.80 (1H, d), 6.57 (1H, d), 4.58 (2H, s), 3.97 (3H, s), 1.43 (18H, s).

Intermediate 18 Methyl 6-[bis-(tert-butoxycarbonyl)amino]-3-(2-hydroxymethyl-furan-3-yl)-2-(4-methylbenzenesulfonyloxy)-benzoate

Sodium borohydride (0.304 g) was added to a solution of methyl 6-[bis-(tert-butoxycarbonyl)amino]-3-(2-formylfuran-3-yl)-2-(4-methylbenzenesulfonyloxy)-benzoate (Intermediate 22, 3.9 g) in ethanol (50 mL) and the mixture was stirred for 15 minutes. The mixture was evaporated to dryness and the residue was partitioned between ethyl acetate and water. The organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness to give methyl 6-[bis-(tert-butoxycarbonyl)amino]-3-(2-hydroxymethylfuran-3-yl)-2-(4-methylbenzene-sulfonyloxy)-benzoate (3.82 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.40 (1H, d), 7.38 (2H, d), 7.30 (1H, d), 7.18 (1H, d), 7.11 (2H, d), 6.28 (1H, d), 4.33 (2H, s), 3.82 (3H, s), 2.40 (3H, s), 1.42 (18H, s).

Intermediate 19 Methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-(2-hydroxy-methylfuran-3-yl)-benzoate

Sodium borohydride (0.031 g) was added to a solution of methyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (Intermediate 28, 0.67 g) in methanol (6 mL) and THF (12 mL) at 0° C. and the resultant mixture was stirred at 0° C. for 10 minutes. Saturated aqueous ammonium chloride, ethyl acetate and water were added and the organic layer was separated, washed with brine, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 30-80% to give methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)-benzoate (0.65 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.66 (1H, s), 7.66-7.62 (3H, m), 7.48 (3H, m), 7.35 (1H, d), 6.58 (1H, d), 6.55 (1H, d), 4.90 (2H, s), 4.56 (2H, s), 3.96 (3H, s).

Intermediate 20 Methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-[2-(1-hydroxy-ethyl)-furan-3-yl]-benzoate

Prepared by proceeding in a similar manner to Intermediate 19, starting from methyl 3-(2-acetylfuran-3-yl)-6-benzenesulfonylmethyl-2-hydroxybenzoate (Intermediate 32).

¹H NMR (CDCl₃) δ: 11.63 (1H, s), 7.64 (3H, dd), 7.47 (3H, m), 7.31 (1H, d), 6.59 (1H, d), 6.47 (1H, d), 4.91-4.89 (2H, m), 4.81 (1H, t), 3.95 (3H, s), 1.54 (3H, s).

Intermediate 21 3-[4-(Benzenesulfonylmethyl)-3-tert-butoxycarbonyl-2-hydroxy-phenyl]-furan-2-carboxylic acid

A solution of sodium phosphate monobasic (0.039 g) in water (1 mL) was added to a solution of tert-butyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (Intermediate 27, 0.105 g) in acetonitrile (2 mL) at 0° C. Hydrogen peroxide (50% wt. in water, 0.078 mL) and sodium chlorite (0.029 g) were added and the reaction mixture was warmed to room temperature and stirred for 18 hours. The mixture was cooled to 0° C. and further sodium phosphate monobasic (0.028 g) in water (0.5 mL), hydrogen peroxide (50% wt. in water, 0.038 mL) and sodium chlorite (0.052 g) were added and the mixture was warmed to room temperature and stirred for 18 hours. The mixture was poured onto sodium sulfite (10% in water) at 0° C., extracted into ethyl acetate, washed with water, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of methanol and 1% acetic acid in methanol with a gradient of O-100%. The resultant product was triturated in cyclohexane and ethyl acetate and the solid was collected by filtration and dried in vacuo to give 3-[4-(benzenesulfonylmethyl)-3-tert-butoxycarbonyl-2-hydroxy-phenyl]-furan-2-carboxylic acid (0.028 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.92 (1H, s), 7.66 (1H, d), 7.56 (3H, m), 7.43 (2H, d), 7.23 (1H, d), 6.75 (1H, d), 6.15 (1H, d), 4.88 (2H, s), 1.70 (9H, s).

Intermediate 22 Methyl 6-[bis-(tert-butoxycarbonyl)amino]-3-(2-formylfuran-3-yl)-2-(4-methylbenzenesulfonyloxy)-benzoate

Triethylamine (0.848 g) was added to a stirred solution of methyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxy benzoate (Intermediate 26, 1.72 g), 4-methylbenzenesulfonyl chloride (1.25 g) and DMAP (0.804 g) in DCM (30 mL) and the resultant mixture was stirred for 1 hour. The mixture was diluted with water and the organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was dissolved in acetonitrile (30 mL) and DMAP (0.804 g) and di-tert-butyl dicarboante (3.16 g) were added. The mixture was stirred for 2 hours then diluted with ethyl acetate and water. The organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 10-50% to give methyl 6-[bis-(tert-butoxycarbonyl)amino]-3-(2-formylfuran-3-yl)-2-(4-methylbenzenesulfonyloxy)-benzoate (3.91 g) as a white foam.

¹H NMR (CDCl₃) δ: 9.13 (1H, d), 7.54 (1H, dd), 7.38 (1H, d), 7.31 (2H, d), 7.23 (1H, d), 7.05 (2H, d), 6.75 (1H, d), 3.94 (3H, s), 2.37 (3H, s), 1.45 (18H, s).

Intermediate 23 Methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-[2-(2-hydroxy-ethyl)-furan-3-yl]-benzoate

A solution of 9-borobicyclononane (0.5M in THF, 12.6 mL) was added to methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-(2-vinylfuran-3-yl)-benzoate (Intermediate 24, 1.0 g) in THF (20 mL) at 50° C. and the resultant mixture was stirred and heated at 50° C. for 75 minutes. After cooling to room temperature, 35% hydrogen peroxide (2 mL) was added and the mixture was stirred for 1.5 hours. Water and ethyl acetate were added to the mixture and the organic layer was separated, washed with water, sodium metabisulfite and brine, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 30-70%. The product was triturated with diethyl ether and the solid was collected by filtration and dried in vacuo to give methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-[2-(2-hydroxyethyl)-furan-3-yl]-benzoate (0.4 g).

¹H NMR (CDCl₃) δ: 11.43 (1H, s), 7.63 (3H, dd), 7.48 (2H, t), 7.43 (1H, d), 7.29 (1H, d), 6.57-6.53 (2H, m), 4.89 (2H, s), 3.94 (3H, s), 3.91 (2H, t), 2.91 (2H, t).

Intermediate 24 Methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-(2-vinylfuran-3-yl)-benzoate

A suspension of methyltriphenylphosphonium bromide (pre-dried under vacuum at 60° C., 3.80 g) in THF (60 mL) was cooled to 5° C., under nitrogen. Potassium bis-(trimethylsilyl)amide (0.5M in toluene, 21.3 mL) was added and the suspension was warmed to room temperature and stirred for 45 minutes. It was cooled to −78° C. and a solution of methyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (Intermediate 28, 1.42 g) in THF (40 mL) was added and the mixture was warmed to room temperature and stirred for 2.5 hours. Ethyl acetate and a saturated aqueous solution of ammonium chloride were added to the mixture and the organic layer was separated, washed with brine, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 15-35% to give methyl 6-(benzenesulfonylmethyl)-2-hydroxy-3-(2-vinylfuran-3-yl)-benzoate (1.24 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.41 (1H, s), 7.63 (3H, dd), 7.48 (2H, m), 7.43 (1H, d), 7.25 (1H, d), 6.67 (1H, d), 6.54 (1H, d), 6.47 (1H, m), 5.77 (1H, dd), 5.22 (1H, dd), 4.90 (2H, s), 3.95 (3H, s).

Intermediate 25 Methyl 6-amino-2-hydroxy-3-[2-(2-hydroxyethyl)-furan-3-yl]-benzoate

Tetrabutylammonium fluoride (1M solution in THF, 25 mL) was added to a solution of methyl 6-amino-3-{2-[2-(tert-butyldimethylsilanyloxy)-ethyl]-furan-3-yl}-2-hydroxybenzoate (Intermediate 29, 1.34 g) in THF (75 mL) and the mixture was stirred for 1 hour. The mixture was evaporated to dryness and water and ethyl acetate were added. The organic layer was separated, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-50% to give methyl 6-amino-2-hydroxy-3-[2-(2-hydroxyethyl)-furan-3-yl]-benzoate (0.88 g) as a yellow gum.

¹H NMR (CDCl₃) δ: 11.70 (1H, s), 7.39 (1H, d), 7.15 (1H, d), 6.46 (1H, d), 6.20 (1H, d), 5.30 (2H, br, s), 4.02 (3H, s), 2.90 (2H, t), 1.26 (2H, t).

Intermediate 26 Methyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate

A mixture of methyl 6-amino-3-bromo-2-hydroxybenzoate (prepared according to Wang et al, Bioorg Med Chem Lett 2007 17 2817, 1.84 g), 2-formylfuran-3-boronic acid pinacol ester (1.99 g), tri-tert-butylphosphinium tetrafluoroborate (0.218 g), cesium carbonate (7.33 g) and tris-(dibenzylideneacetone)dipalladium (0.343 g) in dioxane (75 mL) and water (9.4 mL) was heated at 65° C., under nitrogen, for 1 hour. After cooling, the mixture was diluted with ethyl acetate and water and the organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 10-50% to give methyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (1.72 g) as a yellow solid. The material was used without further characterisation.

Intermediate 27 tert-Butyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-hydroxybenzoate

Prepared by proceeding in a similar manner to Intermediate 26, starting from tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (Intermediate 38) and 2-formylfuran-3-boronic acid pinacol ester

¹H NMR (CDCl₃) δ: 12.03 (1H, s), 9.63 (1H, d), 7.71 (1H, d), 7.65 (3H, d), 7.49 (2H, t), 7.29-7.24 (1H, m), 6.84 (1H, d), 6.29 (1H, d), 4.96 (2H, s), 1.73 (9H, s).

Intermediate 28 Methyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-hydroxybenzoate

Prepared by proceeding in a similar manner to Intermediate 26, starting from methyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (Intermediate 40) and 2-formylfuran-3-boronic acid pinacol ester

¹H NMR (CDCl₃) δ: 11.61 (1H, s), 9.66 (1H, d), 7.72 (1H, dd), 7.65-7.65 (3H, m), 7.51 (2H, m), 7.41 (1H, d), 6.84 (1H, d), 6.59 (1H, d), 4.92 (2H, s), 3.99 (3H, s).

Intermediate 29 Methyl 6-amino-3-{2-[2-(tert-butyldimethylsilanyloxy)-ethyl]-furan-3-yl}-2-hydroxybenzoate

Prepared by proceeding in a similar manner to Intermediate 26, starting from methyl 6-amino-3-bromo-2-hydroxybenzoate (prepared according to Wang et al, Bioorg Med Chem Lett 2007 17 2817) and 2-[2-(tert-butyldimethylsilanyloxy)-ethyl]-furan-3-yl-boronic acid (Intermediate 33). The material was used without further characterisation.

Intermediate 30 Methyl 6-amino-3-(2-formylfuran-3-yl)-2-nitrobenzoate

Prepared by proceeding in a similar manner to Intermediate 26, starting from 6-amino-3-bromo-2-nitrobenzoate (prepared according to Brock et al, Tetrahedron 1963 19 1911) and 2-formylfuran-3-boronic acid pinacol ester.

¹H NMR (DMSO-d₆) δ: 9.45 (1H, d), 8.11 (1H, m), 7.48 (1H, d), 7.06 (1H, d), 6.93 (2H, br, s), 6.67 (1H, d), 3.76 (3H, s).

Intermediate 31 tert-Butyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-(2-hydroxyacetylamino)-benzoate

A mixture of tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-(2-hydroxyacetylamino)benzoate (Intermediate 36, 0.165 g), 2-formylfuran-3-boronic acid pinacol ester (0.091 g), 1,1′-bis(diphenylphosphino)ferrocene palladium dichloride DCM complex (0.028 g) and cesium carbonate (0.311 g) in THF (4.3 mL) and water (0.7 mL) were sealed, under nitrogen, in a microwave vial and heated in the microwave at 140° C. for 10 minutes. After cooling, the mixture was diluted with ethyl acetate and water and the organic layer was separated, washed with brine, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness to give tert-butyl 6-(benzenesulfonylmethyl)-3-(2-formylfuran-3-yl)-2-(2-hydroxyacetylamino)-benzoate (0.17 g).

LCMS (Method A) r/t 3.00 (M+H) 500

Intermediate 32 Methyl 3-(2-acetylfuran-3-yl)-6-(benzenesulfonylmethyl)-2-hydroxybenzoate

A mixture of methyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (Intermediate 40, 0.4 g), 2-acetylfuran-3-boronic acid (0.24 g), tetrakis-(triphenylphosphine) palladium (0.12 g), potassium fluoride monohydrate (0.302 g) and sodium bromide (0.192 g) in α,α,α-trifluorotoluene (8 mL) and dioxane (4 mL) was degassed and then heated in the microwave at 175° C. for 30 minutes. The mixture was cooled and ethyl acetate and water were added. The organic layer was separated, washed with water, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 10-25% to give methyl 3-(2-acetylfuran-3-yl)-6-(benzenesulfonylmethyl)-2-hydroxybenzoate (0.21 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.40 (1H, d), 7.64 (3H, m), 7.58 (1H, d), 7.49 (2H, m), 7.42 (1H, d), 6.74 (1H, d), 6.55 (1H, d), 4.90 (2H, s), 3.95 (3H, s), 2.45 (3H, s).

Intermediate 33 2-[2-(tert-Butyldimethyl silanyloxy)-ethyl]-furan-3-yl-boronic acid

n-Butyllithium (2.5M in hexanes, 5.78 mL) was added to a solution of [2-(3-bromofuran-2-yl)-ethoxy]-tert-butyldimethylsilane (Intermediate 34, 4.01 g) in diethyl ether (130 mL) at −60° C. under nitrogen and the resultant mixture was stirred for 30 minutes. Trimethylborate (2.73 g) was then added to the mixture and it was stirred for a further 10 minutes. The reaction mixture was warmed to 0° C., water was added and the mixture was stirred for 15 minutes. The organic layer was separated, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-30% to give 2-[2-(tert-butyldimethylsilanyloxy)-ethyl]-furan-3-yl-boronic acid (1.23 g) as a colourless oil.

¹H NMR (CDCl₃) δ: 7.28 (1H, d), 6.43 (1H, d), 3.98 (2H, t), 2.97 (2H, t), 1.64-1.50 (3H, m), 1.40-1.37 (3H, m), 0.84-0.81 (9H, m).

Intermediate 34 [2-(3-Bromofuran-2-yl)-ethoxy]-tert-butyldimethylsilane

tert-Butyldimethylsilyl trifluoromethanesulfonate (4.47 g) was added to a solution of 2-(3-bromofuran-2-yl)-ethanol (Intermediate 35, 2.94 g) and pyridine (2.43 g) in DCM (40 mL) and the mixture was stirred for 90 minutes. Water was added and the organic layer was separated, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of DCM and cyclohexane with a gradient of 0-25% to give [2-(3-bromo-furan-2-yl)-ethoxy]-tert-butyldimethylsilane (3.98 g) as a colourless oil. The material was used without further characterisation.

Intermediate 35 2-(3-Bromofuran-2-yl)-ethanol

n-Butyllithium (2.5M in hexanes, 12.9 mL) was added to a solution of 2,3-dibromofuran (6.63 g) in diethyl ether (40 mL) at −78° C. under nitrogen and the mixture was stirred for 15 minutes. A solution of ethylene oxide (15 mL) in diethyl ether (40 mL) was then added. The reaction mixture was stirred for a further 10 minutes then warmed to room temperature and stirred for 30 minutes. Saturated aqueous ammonium chloride was added and the organic layer was separated, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 5-25% to give 2-(3-bromofuran-2-yl)-ethanol (3.81 g) as a yellow oil.

¹H NMR (CDCl₃) δ: 7.31 (1H, d), 6.39 (1H, d), 3.90 (2H, q), 2.94 (2H, t).

Intermediate 36 tert-Butyl 6-(benzenesulfonylmethyl)-3-bromo-2-(2-hydroxy-acetylamino)-benzoate

Sodium hydroxide (0.14 g) was added to a solution of tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-carbamoylmethoxybenzoate (Intermediate 37, 0.33 g) in DMF (5 mL) and the mixture was stirred for 7 hours. Ethyl acetate and a saturated aqueous solution of sodium hydrogen carbonate were added to the mixture and the organic layer was separated, washed with water and brine, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 20-100%, to give tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-(2-hydroxyacetylamino)-benzoate (0.17 g) as a yellow oil.

¹HNMR (CDCl₃) δ: 8.56 (1H, br, s), 7.76 (2H, d), 7.62 (2H, d), 7.54 (2H, t), 6.96 (1H, d), 4.71 (2H, s), 4.31 (2H, s), 1.61 (9H, s).

Intermediate 37 tert-Butyl 6-(benzenesulfonylmethyl)-3-bromo-2-carbamoylmethoxybenzoate

2-Bromoacetamide (0.12 g) and potassium carbonate (0.28 g) were added to solution of tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (Intermediate 38, 0.34 g) in acetone (10 mL) and the mixture was stirred for 18 hours. The mixture was evaporated to dryness and the residue was suspended in DCM and the insoluble material was removed by filtration. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 50-60% to give tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-carbamoylmethoxybenzoate (0.30 g).

¹H NMR (CDCl₃) δ: 7.74-7.68 (2H, m), 7.66 (1H, m), 7.59-7.48 (3H, m), 6.99 (1H, d), 6.73 (1H, br, s), 5.86 (1H, br, s), 4.53 (2H, s), 4.49 (2H, s), 1.58 (9H, s).

Intermediate 38 tert-Butyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxy-benzoate

tert-Butanol (1 mL) and N,N′-dicyclohexylcarbodiimide (0.4 g) were added to a solution of 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoic acid (Intermediate 39, 0.48 g) and DMAP (0.016 g) in THF (10 mL) and the mixture was stirred for 18 hours. It was evaporated to dryness and the residue was suspended in DCM and the insoluble material was removed by filtration. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with DCM to give tert-butyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (0.34 g).

¹H NMR (CDCl₃) δ: 12.09 (1H, s), 7.62-7.55 (3H, m), 7.48 (2H, m), 7.41 (1H, d), 6.07 (1H, d), 4.87 (2H, s), 1.70 (9H, s).

Intermediate 39 6-(Benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoic acid

Prepared by proceeding in a similar manner to Example 1, starting from methyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (Intermediate 40)

LCMS (Method B) r/t 3.16 (M+H) 371/373.

Intermediate 40 Methyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate

Aluminium chloride (2.16 g) was added to a stirred solution of methyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 41, 2.15 g) and N,N-dimethylaniline (3.26 g) in DCM (35 mL) and the resultant mixture was stirred for 50 minutes. Ice water and DCM were added and the organic layer was separated, washed with 1M HCl, dried (Na₂SO₄), filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with DCM to give methyl 6-(benzenesulfonylmethyl)-3-bromo-2-hydroxybenzoate (1.83 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.61 (1H, d), 7.62 (1H, m), 7.59-7.56 (2H, m), 7.53 (1H, d), 7.46-7.45 (2H, m), 6.38 (1H, d), 4.82 (2H, s), 3.93 (3H, s).

Intermediate 41 Methyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoate

A solution of methyl 3-bromo-6-dibromomethyl-2-methoxybenzoate (Intermediate 42A, 19 g) in DMA (300 mL) was added to a stirred solution of sodium benzenesulfinate 17.9 g) and sodium hydrogen carbonate (9.5 g) in water (70 mL) and the mixture was heated at 90° C. for 2 hours. After cooling, the mixture was poured into water and filtered through Celite and the pad was washed with ethyl acetate. The organic layer was separated, washed with water and brine, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 0-100% to give methyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoate (13.8 g).

¹H NMR (CDCl₃) δ: 7.7 (2H, d), 7.65 (1H, t), 7.6 (1H, d), 7.5 (2H, t), 6.95 (1H, d), 4.5 (2H, s), 3.9 (3H, s), 3.85 (3H, s).

Intermediate 42 Methyl 3-bromo-6-dibromomethyl-2-methoxybenzoate (42A) and methyl 3-bromo-6-bromomethyl-2-methoxybenzoate (42B)

Each of two batches containing a solution of methyl 3-bromo-2-methoxy-6-methylbenzoate (Intermediate 43, 30 g), 1,3-dibromo-5,5-dimethylhydantoin (26.54 g) and a catalytic amount of AIBN in 1,2-dichloroethane (500 mL) were heated at 90° C. whilst being illuminated with a 500 W tungsten filament lamp for 40 minutes. After cooling, the solids were removed by filtration and the filtrates were evaporated to dryness. The two residues were combined and purified by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-15% to give methyl 3-bromo-6-dibromomethyl-2-methoxybenzoate (42A, 19 g) as an oil and methyl 3-bromo-6-bromomethyl-2-methoxybenzoate (42B, 54 g) as a crystalline solid.

Intermediate 42A

¹H NMR (CDCl₃) δ: 7.71 (1H, d), 7.66 (1H, d), 6.74 (1H, s), 4.00 (3H, s), 3.90 (3H, s)

Intermediate 42B

¹H NMR (CDCl₃) δ: 7.58 (1H, d), 7.06 (1H, d), 4.47 (2H, s), 3.98 (3H, s), 3.91 (3H, s)

Intermediate 43 Methyl 3-bromo-2-methoxy-6-methylbenzoate

A mixture of methyl 3-bromo-2-hydroxy-6-methylbenzoate (Intermediate 44, 114.5 g), dimethyl sulfate (61 mL) and potassium carbonate (166 g) in acetone (11) was heated at reflux for 2.5 hours. After cooling, the mixture was filtered and the filtrate was evaporated to dryness. The residue was dissolved in DCM and washed with water, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-40%. The product was purified again by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-10%. The product was again purified by chromatography on silica, eluting with a mixture of tert-butyl methyl ether and pentane with a gradient of 0-10% to give methyl 3-bromo-2-methoxy-6-methylbenzoate (66 g).

¹H NMR (CDCl₃) δ: 7.45 (1H, d), 6.85 (1H, d), 3.95 (3H, s), 3.9 (3H, s), 2.25 (3H, s).

Intermediate 44 Methyl 3-bromo-2-hydroxy-6-methylbenzoate

A solution of 1,3-dibromo-5,5-dimethylhydantoin (65 g) in DCM (150 mL) was added dropwise to a stirred and cooled solution of methyl 6-methyl-2-oxocyclohex-3-enecarboxylate (prepared in a similar manner to Hauser et al, Synthesis 1980 814, 75.16 g) and N,N-di-isopropylamine (6.15 mL) in DCM (500 mL) at 0° C. and the resultant mixture was stirred at room temperature for 3 days. The mixture was recooled to 0° C. and further 1,3-dibromo-5,5-dimethylhydantoin (11 g) was added and the mixture was stirred at 0° C. for 3 hours. The precipitate was removed by filtration and the filtrate was evaporated to dryness to give methyl 3-bromo-2-hydroxy-6-methylbenzoate (114.5 g) as an oil.

¹H NMR (CDCl₃) δ: 11.95 (1H, s), 7.55 (1H, d), 6.65 (1H, d), 4.9 (3H, s), 2.5 (3H, s).

Intermediate 45 Methyl 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylate

A solution of methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 4, 0.210 g) in ethanol (6 mL) was added to a flask containing palladium hydroxide (0.020 g) and formic acid (3 drops) under nitrogen. The nitrogen atmosphere was replaced by hydrogen and the mixture was stirred under an atmosphere of hydrogen overnight. The reaction mixture was filtered through Celite and the filtrate was evaporated to dryness. The residue was dissolved in ethyl acetate and washed with 10% aqueous potassium carbonate solution, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-10% to give methyl 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (0.137 g).

¹H NMR (CDCl₃) δ: 7.91 (1H, dd), 7.39 (1H, d), 7.18 (1H, d), 7.07-6.99 (2H, m), 6.93-6.92 (1H, m), 6.56 (1H, d), 5.35 (2H, s), 3.82 (3H, s), 2.92 (2H, t), 2.62-2.52 (6H, m), 1.83 (2H, m), 1.04 (6H, t).

Intermediate 46 Methyl 7-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate

TFA (1 mL) was added to a solution of methyl 7-{N-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)-amino}-furo[2,3-c]chromene-6-carboxylate (Intermediate 47, 0.410 g) in DCM (10 mL). The reaction mixture was stirred at room temperature for 30 minutes. Aqueous potassium carbonate was added and the layers were separated. The organic layer was dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with DMAW 350, followed by DMAW 240 to give methyl 7-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (0.096 g) as a yellow gum.

LCMS (Method D) r/t 2.78 (M+H) 487.

Intermediate 47 Methyl 7-{N-[2((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)-amino}-4H-furo[2,3-c]chromene-6-carboxylate

Methanesulfonyl chloride (0.100 g) was added to an ice-cooled, stirred solution of methyl-7-{N-[4-fluoro-2-((Z)-3-hydroxyprop-1-enyl)benzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 48, 0.413 g) and diisopropylethylamine (0.226 g) in DCM (7 mL). The reaction mixture was stirred with ice cooling for 30 minutes. Ethylamine (2M in THF, 2 mL) was added and the reaction mixture was stirred at room temperature for 5 hours. It was diluted with DCM and washed with water. The organic layer was dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with DMAW 350, followed by DMAW 240 and then DMAW 120. The resultant product was azeotroped with toluene and ethanol to give methyl 7-{N-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (0.401 g) as a dark yellow gum.

¹H NMR (CDCl₃) δ: 7.84 (1H, dd), 7.43 (1H, d), 7.20 (1H, d), 7.04-6.92 (2H, m), 6.88 (1H, d), 6.80 (1H, d), 6.62 (1H, d), 5.90 (1H, m), 5.37 (2H, s), 5.10 (2H, br, s), 3.66 (3H, s), 3.61 (2H, t), 3.48 (2H, dd), 2.79 (2H, q), 1.14 (3H, t), 0.90 (2H, dd), 0.00 (9H, s).

Intermediate 48 Methyl 7-{N-[4-fluoro-2((Z)-3-hydroxyprop-1-enyl)-benzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate

A solution of methyl 7-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(2-trimethylsilanyl-ethoxymethyl)-amino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 49, 3.28 g) and (Z)-3-tributylstannanyl-prop-2-en-1-ol (Intermediate 1, 3.71 g) in dioxane (40 mL) and DMSO (4 mL) was de-gassed and flushed with nitrogen. tris-(Dibenzylideneacetone)dipalladium (0.245 g) and tri-tert-butylphosphonium tetrafluoroborate (0.155 g) were added and the mixture was again de-gassed and flushed with nitrogen. The reaction mixture was heated under nitrogen at 95° C. for 45 minutes. After cooling, the mixture was partitioned between ethyl acetate and water and the organic layer was dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 10-30% to give methyl 7-{N-[4-fluoro-2((Z)-3-hydroxyprop-1-enyl)-benzenesulfonyl]-N-(2-trimethylsilanyl-ethoxymethyl)-amino}-4H-furo[2,3-c]chromene-6-carboxylate (3.01 g) as a white foam.

¹H NMR (CDCl₃) δ: 7.83 (1H, dd), 7.43 (1H, d), 7.20 (1H, d), 7.00 (1H, td), 6.95-6.91 (2H, m), 6.85 (1H, d), 6.61 (1H, d), 5.99-5.95 (1H, m), 5.37 (2H, s), 5.14 (2H, br, s), 4.21-4.15 (2H, t), 3.68 (3H, s), 3.58 (2H, t), 0.88 (2H, m), 0.00 (9H, s).

Intermediate 49 Methyl 7-[N-(2-bromo-4-fluorobenzenesulfonyl)-N-(2-trimethylsilanylethoxymethyl)-amino}-4H-furo[2,3-c]chromene-6-carboxylate

Sodium hydride (60% dispersion in oil, 0.304 g) was added to a stirred solution of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 7, 2.93 g) in THF (30 mL). The resultant mixture was stirred at room temperature for 5 minutes until effervescence had ceased. 2-(trimethylsilyl)ethoxymethyl chloride (1.27 g) was added and the solution was stirred at room temperature for one hour. The mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate, washed with water, dried (Na₂SO₄) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-20% to give methyl 7-[(2-bromo-4-fluorobenzenesulfonyl)-(2-trimethylsilanyl-ethoxymethyl)-amino]-4H-furo[2,3-c]chromene-6-carboxylate (3.51 g) as a white foam.

¹H NMR (CDCl₃) δ: 7.82 (1H, dd), 7.43 (1H, dd), 7.39 (1H, m), 7.22 (1H, d), 7.06 (1H, d), 6.98 (1H, ddd), 6.59 (1H, d), 5.31 (2H, s), 5.28-5.17 (2H, br, s), 3.75-3.67 (2H, m), 3.70 (3H, s), 0.93 (2H, t), 0.00 (9H, s).

Intermediate 50 Methyl 8-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate

Methyl 8-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate (Intermediate 5, 0.147 g) was suspended in ethanol. Formic acid (2 drops) was added and the flask was evacuated and purged with nitrogen gas. Palladium hydroxide (20% wt, 0.015 g) was added and nitrogen was replaced by hydrogen and the mixture was stirred at room temperature under an atmosphere of hydrogen for 1 hour. The mixture was filtered through a pad of Celite and washed with ethanol. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 2.5-10% to give methyl 8-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylate (0.134 g) as a yellow glassy solid.

¹H NMR (CDCl₃) δ: 8.56 (1H, s), 7.87 (1H, dd), 7.50 (1H, d), 7.36 (1H, d), 7.19 (1H, d), 7.06 (1H, dd), 6.94 (1H, m), 6.60 (1H, d), 4.23 (2H, t), 3.81 (3H, s), 3.23 (2H, t), 2.99-2.98 (8H, m), 2.05 (2H, m), 1.24 (6H, t).

Intermediate 51 Methyl 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate

TFA (2 mL) was added to a solution of methyl 7-{N-[4-fluoro-2-((Z)-3-{morpholin-4-yl}prop-1-enyl)benzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 52, 1.15 g) in DCM (20 mL). The reaction mixture was stirred at room temperature for 30 minutes. Aqueous potassium carbonate was added and the layers were separated. The organic layer was dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 20-80% to give methyl 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (0.412 g) as a yellow foam.

¹H NMR (CDCl₃) δ: 8.08 (1H, dd), 7.39 (1H, d), 7.15 (1H, d), 7.11-7.03 (2H, m), 6.99 (1H, d), 6.90 (1H, d), 6.54 (1H, d), 6.00 (1H, dt), 5.36 (2H, s), 3.87 (3H, s), 3.62 (4H, t), 2.95 (2H, br, m), 2.33 (4H, br, s).

Intermediate 52 Methyl 7-{N-[4-fluoro-2-((Z)-3-{morpholin-4-yl}prop-1-enyl)-benzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate

Methanesulfonyl chloride (0.100 g) was added to an ice-cooled, stirred solution of methyl-7-{N-[4-fluoro-2-((Z)-3-hydroxyprop-1-enyl)benzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 48, 1.57 g) and diisopropylethylamine (0.859 g) in DCM (25 mL) and the mixture was stirred in an ice bath for 20 minutes. Morpholine (0.689 g) was added and the reaction mixture was stirred at room temperature for 90 minutes. It was washed with water, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 10-80% to give methyl 7-{N-[4-fluoro-2((Z)-3-{morpholin-4-yl}prop-1-enyl)benzenesulfonyl]-N-(2-trimethylsilanylethoxy-methyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (1.15 g) as a yellow gum.

¹H NMR (CDCl₃) δ: 7.82 (1H, dd), 7.43 (1H, d), 7.19 (1H, d), 7.09 (1H, dd), 7.00-6.94 (1H, m), 6.89 (1H, d), 6.81 (1H, d), 6.61 (1H, d), 5.91-5.83 (1H, m), 5.37 (2H, s), 5.12 (2H, br, s), 3.72-3.66 (4H, m), 3.68 (3H, s), 3.63 (2H, t), 3.04 (2H, dd), 2.42 (4H, s), 0.91 (2H, dd), 0.00 (9H, s).

Intermediate 53 Methyl 7-{4-fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate

A mixture of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 7, 0.300 g) and 1-((Z)-3-tributylstannanyl-allyl)-pyrrolidine (Intermediate 54, 0.390 g) in DMSO (2 mL) and dioxane (8 mL) was de-gassed and purged with nitrogen before tris-(dibenzylideneacetone)dipalladium (0) (0.076 g) and tri-tert-butylphosphonium tetrafluoroborate (0.048 g) were added and the mixture was heated at 90° C. for 3 hours. After cooling, the mixture was diluted with ethyl acetate and filtered. The filtrate was washed with water, dried (MgSO₄), and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-10%. The resultant product was triturated with ether to give methyl 7-{4-fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]benzenesulfonyl-amino}-4H-furo[2,3-c]chromene-6-carboxylate (0.124 g), as a pale orange solid.

¹H NMR (CD₃OD) δ: 8.02 (1H, dd), 7.51 (1H, m), 7.16 (2H, d), 7.11-7.01 (2H, m), 6.76 (1H, d), 6.69 (1H, d), 5.93-5.83 (1H, m), 5.31 (2H, s), 3.80 (3H, s), 3.37-3.33 (2H, m), 2.69 (4H, m), 1.78 (4H, m).

Intermediate 54 1-((Z)-3-Tributylstannanylallyl)-pyrrolidine

Prepared by proceeding in a similar manner to Intermediate 3, starting from ((Z)-3-bromoprop-1-enyl)tributylstannane (Intermediate 2) and pyrrolidine.

¹H NMR (CDCl₃) δ: 6.64 (1H, dt), 5.96 (1H, dt), 3.10 (2H, dd), 2.51 (4H, m), 1.79-1.78 (4H, m), 1.54-1.45 (6H, m), 1.36-1.26 (6H, m), 0.91-0.88 (15H, t).

Intermediate 553 tert-Butyl 7-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate

A suspension of tert-butyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 56, 0.330 g) and N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3, 0.493 g) in dioxane was warmed slightly then de-gassed and purged with nitrogen. tris-(Dibenzylideneacetone)dipalladium (0.056 g) and tri-tert-butylphosphonium tetrafluoroborate (0.036 g) were added and the mixture was de-gassed and purged with nitrogen again. The resultant mixture was heated at 95° C., under an atmosphere of nitrogen for 75 minutes. This was cooled and concentrated in vacuo and the residue was partitioned between water and ethyl acetate (2×). The combined organic layers were dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with methanol and DCM, with a gradient of 0-25%. The product was triturated with ether and the resultant product was dried in vacuo at 50° C. overnight to give tert-butyl 7-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (0.215 g) as a sand coloured solid.

¹H NMR (CDCl₃) δ: 8.16 (1H, dd), 7.87 (1H, d), 7.64 (1H, d), 7.40 (1H, d), 7.11 (1H, td), 7.03 (2H, m), 6.93 (1H, d), 6.15-6.06 (1H, m), 3.19 (2H, br, d), 2.62-2.53 (4H, m), 1.67 (9H, s), 0.95 (6H, t).

Intermediate 56 tert-Butyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate

2-Bromo-4-fluorobenzenesulfonyl chloride (0.229 g) was added to a solution of tert-butyl 7-amino-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 57, 0.210 g) and pyridine (1.13 mL) in DCM (20 mL) and the mixture was stirred at room temperature overnight. The mixture was reduced to half volume in vacuo and the resultant mixture was stirred and heated at 35° C. for 6 hours. Further 2-bromo-4-fluorobenzenesulfonyl chloride (0.572 g) was added and the reaction mixture was heated at 35° C. overnight. The mixture was evaporated to dryness and the residue was partitioned between water and ethyl acetate. The combined organic layers were dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with ethyl acetate and cyclohexane, with a gradient of 5-20% to give tert-butyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (0.329 g) as a white solid.

¹H NMR (CDCl₃) δ: 8.30 (1H, dd), 7.88 (1H, d), 7.65 (1H, d), 7.53 (1H, d), 7.44 (1H, dd), 7.21-7.13 (1H, m), 6.93 (1H, d), 1.71 (9H, s).

Intermediate 57 tert-Butyl 7-amino-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate

To a solution of tert-butyl 7-benzyloxycarbonylamino-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 58, 0.318 g) in ethyl acetate (10 mL) was added a slurry of 10% palladium on activated carbon (0.032 g) in ethyl acetate (10 mL). The flask was de-gassed and filled with hydrogen and the mixture stirred at room temperature for 90 minutes. The mixture was filtered through Celite and washed with ethyl acetate. The filtrate was concentrated in vacuo to give tert-butyl 7-amino-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (0.214 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.81 (1H, d), 7.49 (1H, d), 6.87 (1H, d), 6.64 (1H, d), 1.68 (9H, s).

Intermediate 58 tert-Butyl 7-benzyloxycarbonylamino-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate

To a solution of 4-(4-benzyloxycarbonylamino-3-tert-butoxycarbonyl-2-hydroxyphenyl)-furan-3-carboxylic acid (Intermediate 59, 0.382 g) and DMAP (0.005 g) in THF (25 mL) was added dicyclohexylcarbodiimide (0.209 g). The reaction mixture was stirred at room temperature for 3 hours and the resultant white precipitate was filtered off and washed with ethyl acetate. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 5-20% to give tert-butyl 7-benzyloxycarbonylamino-4-oxo-4H-furo[2,3-c]chromene-6-carboxylate (0.318 g) as a white solid.

¹H NMR (CDCl₃) δ: 9.26 (1H, s), 8.34 (1H, d), 7.88 (1H, d), 7.75 (1H, d), 7.45-7.33 (5H, m), 6.99 (1H, d), 5.24 (2H, s), 1.68 (9H, s).

Intermediate 59 3-(4-Benzyloxycarbonylamino-3-tert-butoxycarbonyl-2-hydroxyphenyl)-furan-2-carboxylic acid

A solution of sodium chlorite (0.113 g) and sodium phosphate monobasic (0.168 g) in water (51 mL) was added to a suspension of tert-butyl 6-benzyloxycarbonylamino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (Intermediate 60, 0.438 g) and 2-methyl-2-butene (1.06 mL) in tert-butanol (25 mL) and acetonitrile (5 mL). The reaction mixture was stirred at room temperature. Further amounts of sodium chlorite (0.137 g) and sodium phosphate monobasic (0.180 g), in water (4 mL) were added and the reaction mixture was stirred at room temperature for 4.5 hours. The resultant mixture was basified to pH 10 with 1M sodium hydroxide solution and the mixture was concentrated in vacuo. Water (15 mL) was added and the mixture was extracted with ethyl acetate. The aqueous layer was acidified to pH 2 with 1M hydrochloric acid and extracted with ethyl acetate. The combined organic layers were dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-15% to give 3-(4-benzyloxycarbonylamino-3-tert-butoxycarbonyl-2-hydroxyphenyl)-furan-2-carboxylic acid (0.385 g) as a yellow oil which solidified on standing.

¹H NMR (CDCl₃) δ: 9.75 (1H, s), 7.95 (1H, d), 7.62 (1H, d), 7.50 (1H, d), 7.41-7.37 (5H, m), 6.70 (1H, d), 5.22 (2H, s), 1.67 (9H, s).

Intermediate 60 tert-Butyl 6-benzyloxycarbonylamino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate

Benzyl chloroformate (0.528 g) was added to a stirred solution of tert-butyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (Intermediate 61, 0.854 g) in diethyl ether (20 mL). The reaction mixture was stirred at room temperature for 2 hours. A further amount of benzyl chloroformate (1.056 g) was added and the resultant mixture stirred at room temperature overnight. The mixture was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 5-15% to give tert-butyl 6-benzyloxycarbonylamino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (0.588 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 11.87 (1H, s), 9.76 (1H, s), 9.65 (1H, d), 8.01 (1H, d), 7.68 (1H, dd), 7.48 (1H, d), 7.41-7.34 (5H, m), 6.77 (1H, d), 5.23 (2H, s), 1.68 (9H, s).

Intermediate 61 tert-Butyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate

A mixture of tert-butyl 6-amino-3-bromo-2-hydroxybenzoate (Intermediate 62, 1.16 g), 2-formylfuran-3-boronic acid pinacol ester (1.073 g), tris-(dibenzylideneacetone)dipalladium (0.184 g), tri-tert-butylphosphonium tetrafluoroborate (0.117 g) and cesium carbonate (3.935 g) was suspended in dioxane (40 mL) and water (5 mL). The mixture was de-gassed and flushed with nitrogen then heated at 70° C. for 3 hours. After cooling, the mixture was concentrated in vacuo. The residue was partitioned between water and ethyl acetate and the combined organic layers were dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 2.5-25% to give tert-butyl 6-amino-3-(2-formylfuran-3-yl)-2-hydroxybenzoate (0.854 g) as a yellow oil.

¹H NMR (CDCl₃) δ: 12.11 (1H, s), 9.66 (1H, d), 7.64 (1H, dd), 7.25 (1H, d), 6.79 (1H, d), 6.21 (1H, d), 5.52 (2H, s), 1.67 (9H, s).

Intermediate 62 tert-Butyl 6-amino-3-bromo-2-hydroxybenzoate

Dicyclohexylcarbodiimide (4.14 g) was added to a stirred solution of 6-amino-3-bromo-2-hydroxybenzoic acid (Intermediate 63, 3.88 g) and DMAP (0.102 g) in tert-butanol (20 mL) and THF (150 mL). The mixture was stirred at room temperature for 4 hours. The resultant white precipitate was filtered off and washed with ethyl acetate. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 2.5-15% to give tert-butyl 6-amino-3-bromo-2-hydroxybenzoate (1.16 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 11.99 (1H, s), 7.30 (1H, d), 6.06 (1H, d), 5.35 (2H, s), 1.65 (9H, s).

Intermediate 63 6-Amino-3-bromo-2-hydroxybenzoic acid

A mixture of methyl 6-amino-3-bromo-2-hydroxybenzoate (prepared according to Wang et al, Bioorg Med Chem Lett 2007 17 2817, 5.41 g) and lithium hydroxide monohydrate (9.23 g) was suspended in dioxane (100 mL) and water (100 mL) and heated at 80° C. overnight. The temperature was then increased to 100° C. for 4 hours. A further amount of lithium hydroxide monohydrate (4.61 g) was added and the reaction mixture was heated at 100° C. for a further 1 hour. After cooling, the mixture was concentrated in vacuo and the residue was acidified to pH3 with formic acid and extracted with ethyl acetate. The organic layer was dried (MgSO₄), filtered and the filtrate was concentrated in vacuo to give 6-amino-3-bromo-2-hydroxybenzoic acid (6.22 g) as a black/grey solid.

¹H NMR (DMSO-d₆) δ: 7.24 (1H, d), 6.16 (1H, d).

Intermediate 64 Methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylate

Diisopropyl azodicarboxylate (0.067 g) was added to a solution of methyl 6-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxy-3-[2-(1-hydroxyethyl)-furan-3-yl]-benzoate (Intermediate 65, 0.180 g) and triphenyl phosphine (0.087 g) in THF (2 mL), at 10° C. The resultant mixture was stirred as the temperature rose to room temperature over 45 minutes. It was then concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-15% to give methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylate (0.070 g) as a gum.

¹H NMR (CDCl₃) δ: 7.89 (1H, dd), 7.41 (1H, dd), 7.20-7.11 (2H, m), 7.09-7.01 (2H, m), 6.71 (1H, d), 6.60 (1H, d), 6.16 (1H, dt), 5.60 (1H, q), 4.55 (2H, s), 3.89 (3H, s), 3.34 (2H, d), 2.67 (4H, q), 1.62 (3H, d), 1.06 (6H, t).

Intermediate 65 Methyl 6-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxy-3-[2-(1-hydroxyethyl)-furan-3-yl]-benzoate

A solution of methyl 3-(2-acetylfuran-3-yl)-6-[2((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxybenzoate (Intermediate 66, 0.862 g) in methanol (9 mL) was added to a suspension of sodium borohydride (0.121 g) in THF (9 mL), at −10° C., over 10 minutes. The resultant mixture was stirred and gradually warmed to just below room temperature, then quenched by the addition of saturated ammonium chloride solution. The mixture was extracted with ethyl acetate, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo to give methyl 6-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxy-3-[2-(1-hydroxyethyl)-furan-3-yl]-benzoate (0.820 g) as a foam.

¹H NMR (CDCl₃) δ: 7.81 (1H, dd), 7.44 (1H, d), 7.28 (2H, m), 7.09 (2H, br, m), 6.48 (1H, d), 6.45 (1H, d), 6.12 (1H, br, m), 4.91 (2H, q), 4.81 (1H, q), 3.99 (3H, s), 3.36 (2H, br, m), 2.78 (4H, br, m), 1.55 (3H, d), 1.08 (6H, br, m).

Intermediate 66 Methyl 3-(2-acetylfuran-3-yl)-6-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxybenzoate

A mixture of methyl 3-bromo-6-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxybenzoate (Intermediate 67, 0.880 g), 2-acetylfuran-3-boronic acid (Intermediate 68, 0.300 g), tris-(dibenzylideneacetone)-dipalladium (0.075 g), tri-tert-butylphosphonium tetrafluoroborate (0.050 g) and cesium carbonate (1.61 g) in dioxane (22 mL) and water (2.6 mL) was de-gassed, purged with nitrogen and heated at 65° C. for 1 hour. The mixture was cooled, diluted with ethyl acetate and filtered through Celite and washed with ethyl acetate. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-15% to give methyl 3-(4-acetylfuran-3-yl)-6-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxybenzoate (0.870 g) as a gum.

¹H NMR (CDCl₃) δ: 7.74 (1H, dd), 7.57 (1H, d), 7.38 (1H, d), 7.23-7.18 (1H, br, d), 7.17-7.07 (1H, br, m), 7.03 (1H, td) 6.73 (1H, d), 6.39 (1H, d), 6.15 (1H, m), 4.91 (2H, s), 4.01 (3H, s), 3.27 (2H, br, d), 2.59 (4H, br, q), 2.44 (3H, s), 1.04 (6H, t).

Intermediate 67 Methyl 3-bromo-6-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxybenzoate

A solution of methyl 3-bromo-6-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-methoxybenzoate (Intermediate 69, 3.9 g) and N,N-dimethylaniline (9.00 g) in DCM (150 mL) was cooled to 0° C. and aluminium chloride (3.00 g) was added in three portions. The resultant mixture was stirred at room temperature for 2 hours. The mixture was cooled in an ice bath and quenched with brine. The layers were separated and the organic phase was dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. Cyclohexane was added to the residual gum and then decanted off. The residual oil was dissolved in DCM and concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-15% to give methyl 3-bromo-6-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-hydroxybenzoate (2.52 g) as a blue glass.

¹H NMR (CDCl₃) δ: 11.44 (1H, s), 7.76 (1H, dd), 7.57 (1H, d), 7.16 (1H, t), 6.91 (1H, d), 6.72 (1H, d), 6.37 (1H, d), 6.33 (1H, m), 4.87 (2H, s), 3.98 (3H, s), 3.63 (2H, br, m), 3.05 (4H, br, m), 1.27 (6H, s).

Intermediate 68 2-Acetylfuran-3-boronic acid

2,3-Dibromofuran (5.00 g) was dissolved in anhydrous diethyl ether (200 mL) and cooled to −70° C., under an atmosphere of nitrogen. n-Butyllithium (2.5M solution in hexanes, 10.2 mL) was added and the resultant mixture was stirred at −70° C. for 50 minutes. A solution of anhydrous N,N-dimethylacetamide (2.3 mL) in diethyl ether (20 mL) was added and the mixture was warmed to −10° C. The solution was re-cooled to −70° C. and n-butyllithium (2.5M solution in hexanes, 11 mL) was added and the resultant mixture stirred at −70° C. for 1 hour. Tri-isopropyl borate (6.2 mL) was added and the reaction mixture was stirred while the temperature rose from −70° C. to 0° C. The mixture was acidified with 4M hydrochloric acid, extracted into ether, dried (MgSO₄) and filtered. The filtrate was concentrated to give an oil which was triturated with tert-butyl methyl ether and the solid obtained was collected by filtration and dried under vacuum to give 2-acetyl-furan-3-boronic acid (0.760 g) as a brown solid.

¹H NMR (CDCl₃) δ: 7.54 (1H, d), 7.34 (2H, br, s), 6.85 (1H, d), 2.57 (3H, s).

Intermediate 69 Methyl 3-bromo-6-[2((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-methoxybenzoate

A mixture of methyl 3-bromo-6-(2-bromo-4-fluorobenzenesulfonylmethyl)-2-methoxybenzoate (Intermediate 70, 5.85 g), N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3, 5.00 g) and cesium fluoride (3.29 g) in THF (100 mL) was de-gassed and purged with nitrogen for 5 minutes. Palladium tetrakis-(triphenylphosphine) (0.720 g) was added and the reaction mixture was heated at reflux overnight. The mixture was cooled, diluted with ethyl acetate, filtered through Celite and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-10% to give methyl 3-bromo-6-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-2-methoxybenzoate (3.9 g) as an oil.

¹H NMR (CDCl₃) δ: 7.89 (1H, dd), 7.55 (1H, d), 7.25 (1H, d), 7.09 (2H, m), 6.81 (1H, d), 6.15 (1H, m), 4.53 (2H, s), 3.95 (3H, s), 3.91 (3H, s), 3.23 (2H, d), 2.56 (4H, q), 1.01 (6H, t).

Intermediate 70 Methyl 3-bromo-6-(2-bromo-4-fluorobenzenesulfonylmethyl)-2-methoxybenzoate

A mixture of 2-bromo-4-fluorothiophenol (3.21 g), methyl 3-bromo-6-bromomethyl-2-methoxybenzoate (Intermediate 42B, 5.00 g) and potassium carbonate (5.00 g) in THF (100 mL) was heated at reflux for 1 hour. The resultant mixture was cooled, filtered and concentrated in vacuo. The residue was dissolved in acetic acid (80 mL), hydrogen peroxide (10%, 10 mL) was added. The reaction mixture was heated at 80° C. for 2 hours and then stirred at room temperature overnight. The mixture was diluted with water and extracted with DCM. The organic phase was washed with saturated sodium metabisulfite solution, saturated sodium bicarbonate solution and brine, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo to give methyl 3-bromo-6-(2-bromo-4-fluorobenzenesulfonylmethyl)-2-methoxybenzoate (7.3 g) as a glass.

¹H NMR (CDCl₃) δ: 7.88 (1H, dd), 7.55 (1H, d), 7.52 (1H, dd), 7.11 (1H, ddd), 6.94 (1H, d), 4.80 (2H, s), 3.94 (3H, s), 3.86 (3H, s).

Intermediate 71 Methyl 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylate

A mixture of methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylate (Intermediate 6, 0.180 g) and palladium hydroxide on carbon (˜0.005 g) in acetic acid (2 mL) and dioxane (20 mL) was stirred at room temperature under an atmosphere of hydrogen for 2 hours. The resultant mixture was filtered through Celite and washed with ethyl acetate. The filtrate was concentrated in vacuo to give methyl 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylate (0.100 g) as a gum which was used without further characterisation.

Intermediate 72 Methyl 7-[2((Z)-3-diethylaminopropl-enyl)-4-fluorobenzenesulfonylamino]-4H-chromeno[3,4-d]isothiazole-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 55, starting from methyl-7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-chromeno[3,4-d]isothiazole-6-carboxylate (Intermediate 73).

¹H NMR (CDCl₃) δ: 8.26 (1H, s), 8.16 (1H, dd), 7.33 (1H, d), 7.15 (1H, td), 7.08-7.01 (3H, m), 6.23-6.14 (1H, m), 5.40 (2H, s), 3.95 (3H, s), 3.24 (2H, br, d), 2.64 (4H, br, q), 1.03 (6H, t).

Intermediate 73 Methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-chromeno[3,4-d]isothiazole-6-carboxylate

To a stirred solution of methyl 7-amino-4H-chromeno[3,4-d]isothiazole-6-carboxylate (Intermediate 74, 0.300 g) in DCM (15 mL) was added pyridine (2.5 mL), followed by 2-bromo-4-fluorobenzenesulfonyl chloride (0.468 g). The resultant mixture was stirred at room temperature overnight. A further amount of 2-bromo-4-fluorobenzenesulfonyl chloride (0.300 g) was added and stirring was continued overnight. The mixture was diluted with DCM and washed with 0.5M hydrochloric acid and aqueous sodium bicarbonate. The organic layer was dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 15-45% to give methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-chromeno[3,4-d]isothiazole-6-carboxylate (0.460 g) as a cream solid.

¹H NMR (CDCl₃) δ: 9.84 (1H, br, s), 8.25 (1H, s), 8.24-8.20 (1H, dd), 7.43 (1H, dd), 7.33 (1H, d), 7.20-7.12 (2H, m), 5.40 (2H, s), 3.97 (3H, s).

Intermediate 74 Methyl 7-amino-4H-chromeno[3,4-d]isothiazole-6-carboxylate

A suspension of methyl 7-tert-butylcarbonylamino-4H-chromeno[3,4-d]isothiazole-6-carboxylate (Intermediate 75, 0.690 g) in methanol (30 mL) was treated with concentrated sulfuric acid (1.2 mL) and the resultant mixture was heated at 75° C. in a sealed vessel overnight. The mixture was cooled, diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate solution. The aqueous phase was saturated with sodium chloride then extracted with ethyl acetate again. The combined organic layers were dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 15-45% to give methyl 7-amino-4H-chromeno[3,4-d]isothiazole-6-carboxylate (0.345 g) as a yellow solid.

¹H NMR (CD₃OD) δ: 8.25 (1H, s), 7.30 (1H, d), 6.44 (1H, d), 5.33 (2H, s), 3.87 (3H, s).

Intermediate 75 Methyl 7-tert-butylcarbonylamino-4H-chromeno[3,4-d]isothiazole-6-carboxylate

Ammonium thiocyanate (0.595 g) was added to a stirred solution of methyl 7-tert-butylcarbonylamino-4-chloro-3-formyl-2H-chromene-8-carboxylate (Intermediate 76, 1.10 g) in acetone (25 mL) and the resultant mixture was stirred at 60° C. for 90 minutes. The mixture was cooled, diluted with DCM and washed with saturated sodium bicarbonate solution. The aqueous phase was extracted with DCM and the combined organic layers were washed with brine, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 10-25% to give 7 methyl 7-tert-butylcarbonylamino-4H-chromeno[3,4-d]isothiazole-6-carboxylate (0.730 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 10.10 (1H, br, s), 8.28 (1H, s), 8.26 (1H, d), 7.48 (1H, d), 5.42 (2H, s), 3.98 (3H, s), 1.33 (9H, s).

Intermediate 76 Methyl 7-tert-butylcarbonylamino-4-chloro-3-formyl-2H-chromene-8-carboxylate

A suspension of methyl 7-tert-butylcarbonylamino-4-oxochroman-8-carboxylate (Intermediate 77, 1.32 g) in trichloroethylene (25 mL) was treated with DMF (1.5 mL), followed by dropwise addition of phosphorus oxychloride (0.998 g). The resultant mixture was heated at 60° C. for 2 hours. A further amount of phosphorus oxychloride (0.200 g) was added and the mixture was heated at 60° C. for 40 minutes. After cooling, the mixture was diluted with DCM and washed with saturated aqueous sodium bicarbonate solution. The aqueous phase was extracted with DCM and the combined organic layers were washed with brine, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-25% to give methyl 7-tert-butylcarbonylamino-4-chloro-3-formyl-2H-chromene-8-carboxylate (1.175 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 10.41 (1H, br, s), 10.12 (1H, s), 8.35 (1H, d), 7.79 (1H, d), 5.01 (2H, s), 3.94 (3H, s), 1.31 (9H, s).

Intermediate 77 Methyl 7-tert-butylcarbonylamino-4-oxochroman-8-carboxylate

A solution of methyl 2-tert-butylcarbonylamino-6-(2-carboxyethoxy)-benzoate (Intermediate 78, 2.73 g) in DCM (50 mL) was stirred at room temperature. DMF (5 drops) was added, followed by oxalyl chloride (2.0 g). After 30 minutes of stirring, the mixture was concentrated in vacuo and the residue was redissolved in DCM and evaporated to dryness. The residue was dissolved in DCM (50 mL) and aluminium chloride (3.38 g) was added. The resultant mixture was stirred at room temperature for 5 hours then diluted with more DCM and washed with ice/water. After separation, the aqueous phase was extracted with more DCM and the combined organic layers were washed with saturated aqueous sodium bicarbonate, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 10-40% to give methyl 7-tert-butylcarbonylamino-4-oxochroman-8-carboxylate (1.16 g) as a white crystalline solid.

¹H NMR (CDCl₃) δ: 10.50 (1H, br, s), 8.31 (1H, d), 8.04 (1H, dd), 4.59 (2H, t), 3.97 (3H, s), 2.82 (2H, t), 1.32 (9H, s).

Intermediate 78 Methyl 2-tert-butylcarbonylamino-6-(2-carboxyethoxy)-benzoate

Potassium tert-butoxide (1.81 g) was added to a solution of methyl 2-tert-butylcarbonylamino-6-hydroxybenzoate (Intermediate 79, 4.06 g) in THF (30 mL) and the mixture was heated at 60° C. β-propiolactone (1.16 g) was added dropwise and the resultant mixture was heated at 60° C. for 25 minutes, then left to stand at room temperature overnight. Ethyl acetate and water were added and the layers were separated. The aqueous phase was extracted with more ethyl acetate and acidified to pH 2 using 1M hydrochloric acid. This was extracted with ethyl acetate, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 50-100% to give methyl 2-tert-butylcarbonylamino-6-(2-carboxyethoxy)-benzoate (3.5 g) as a white solid.

¹H NMR (CDCl₃) δ: 9.97 (1H, br, s), 8.13 (1H, dd), 7.39 (1H, t), 6.70 (1H, dd), 4.31 (2H, t), 3.89 (3H, s), 2.85 (2H, t), 1.30 (9H, s).

Intermediate 79 Methyl 2-tert-Butylcarbonylamino-6-hydroxybenzoate

A solution of methyl 2-amino-6-hydroxybenzoate (prepared according to Comess et al, US2004 167128, 3.8 g) and sodium bicarbonate (2.52 g) in ethyl acetate (75 mL) and water (17.5 mL) was stirred at room temperature and pivaloyl chloride (3.51 g) was added dropwise. The resultant mixture was stirred at room temperature for 1 hour. A further amount of pivaloyl chloride (1.75 g) was added and the mixture was stirred at room temperature for 2.5 hours. A further amount of pivaloyl chloride (1 g) was added and the mixture was stirred at room temperature for 4 hours and 20 minutes. Ethyl acetate and saturated aqueous sodium bicarbonate solution were added and the layers were separated. The organic phase was washed with brine, dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 5-25% to give methyl 2-tert-butylcarbonylamino-6-hydroxybenzoate (4.46 g) as a white solid.

¹H NMR (CDCl₃) δ: 10.42 (1H, s), 10.33 (1H, br, s), 8.22 (1H, dd), 7.41 (1H, t), 6.72 (1H, dd), 4.09 (3H, s), 1.33 (9H, s).

Intermediate 80 Methyl 7-[2((Z)-3-diethylaminoprop-1-enyl)-benzenesulfonyl-amino-4H-furo[2,3-c]chromene-6-carboxylate

A mixture of methyl 7-(2-bromobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 81, 0.140 g) and N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3, 0.243 g) in dioxane (5 mL) was de-gassed and purged with argon for several minutes. tris-(Dibenzylideneacetone)dipalladium (0.028 g) and tri-tert-butylphosphonium tetrafluoroborate (0.017 g) were added and the solution was de-gassed, purged with argon. The mixture was heated at 95° C. for 1 hour then cooled and concentrated in vacuo. The residue was partitioned between ethyl acetate and water and the organic layer was dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 2.5-20% to give methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-benzenesulfonylamino-4H-furo[2,3-c]chromene-6-carboxylate (0.050 g) as a brown solid.

¹H NMR (CDCl₃) δ: 8.06 (1H, dd), 7.54 (1H, td), 7.45-7.38 (2H, m), 7.29 (1H, d), 7.16 (1H, d), 7.03 (1H, d), 6.96 (1H, d), 6.55 (1H, d), 6.07-5.98 (1H, m), 5.36 (2H, s), 3.87 (3H, s), 3.24 (2H, br, s), 2.59 (4H, br, s), 0.95 (6H, m).

Intermediate 81 Methyl 7-(2-bromobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate

A suspension of methyl 7-[bis-(tert-butoxycarbonyl)amino]-4H-furo[2,3-c]-chromene-6-carboxylate (Intermediate 10, 0.500 g) in formic acid (6 mL) was stirred at room temperature for 2 hours. The formic acid was removed in vacuo and the residue was partitioned between saturated aqueous potassium carbonate solution and ethyl acetate. The organic layer was dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was suspended in DCM (2 mL) and pyridine (1.82 mL) and 2-bromobenzenesulfonyl chloride (0.344 g) were added. The reaction mixture was stirred at room temperature overnight. The mixture was concentrated in vacuo and the residue was partitioned between water and DCM. The organic layer was dried by phase separation and concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 5-15% to give methyl 7-(2-bromobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (0.279 g) as a yellow solid.

¹H NMR (CDCl₃) δ: 9.24 (1H, s), 8.14 (1H, dd), 7.68 (1H, dd), 7.46-7.33 (3H, m), 7.15 (2H, d), 6.54 (1H, d), 5.36 (2H, s), 3.93 (3H, s).

Intermediate 82 Methyl 7-{4-fluoro-2-[(Z)-3-((R)-3-acetoxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate

A mixture of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 7, 0.09 g) and acetic acid (R)-1-((Z)-3-tributylstannylallyl)-pyrrolidin-3-yl ester (Intermediate 83, 0.170 g) in dioxane (4.5 mL) and DMSO (0.5 mL) was de-gassed and purged with argon for several minutes. tris-(Dibenzylideneacetone)dipalladium (0.017 g) and tri-tert-butylphosphonium tetrafluoroborate (0.011 g) were added and the solution was de-gassed, purged with argon and then heated at 50° C. for 2 hours. After cooling, the mixture was diluted with ethyl acetate and filtered through Celite. The filtrate was washed with water, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-10% to give methyl 7-{4-fluoro-2-[(Z)-3-((R)-3-acetoxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (0.092 g) as a thick yellow oil which was used without further characterisation.

Intermediate 83 Acetic acid (R)-1-((Z)-3-tributylstannanylallyl)-pyrrolidin-3-yl ester

Prepared by proceeding in a similar manner to Intermediate 3, starting from ((Z)-3-bromoprop-1-en-1-yl)-tributyl-stannane (Intermediate 2) and acetic acid (R)-pyrrolidin-3-yl ester.

¹H NMR (CDCl₃) δ: 6.62 (1H, dt), 6.00 (1H, d), 5.21-5.13 (1H, m), 3.11 (2H, t), 2.83 (1H, m), 2.72 (2H, m), 2.43-2.19 (2H, m), 2.04 (3H, s), 1.91-1.79 (1H, m), 1.56-1.39 (6H, m), 1.37-1.23 (6H, m), 0.89 (15H, m).

Intermediate 84 Methyl 7-{4-fluoro-2-[(Z)-3-((S)-3-acetoxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 82, starting from methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 7) and acetic acid (S)-1-((Z)-3-tributylstannanylallyl)-pyrrolidin-3-yl ester (Intermediate 85).

¹H NMR (CDCl₃) δ: 8.07 (1H, m), 7.40 (1H, m), 7.15 (1H, m), 7.11-7.02 (2H, m), 6.96-6.88 (2H, m), 6.55 (1H, d), 6.09-6.00 (1H, m), 5.37 (2H, s), 5.13-5.03 (1H, m), 3.88 (3H, s), 3.05 (2H, m), 2.80-2.52 (3H, m), 2.30-2.09 (2H, m), 2.00 (3H, s), 1.81-1.71 (1H, m).

Intermediate 85 Acetic acid (S)-1-((Z)-3-tributylstannanylallyl)-pyrrolidin-3-yl ester

Prepared by proceeding in a similar manner to Intermediate 3, starting from ((Z)-3-bromoprop-1-en-1-yl)-tributyl-stannane (Intermediate 2) and acetic acid (S)-pyrrolidin-3-yl ester.

¹H NMR (CDCl₃) δ: 6.62 (1H, dt), 6.00 (1H, d), 5.18 (1H, m), 3.11 (2H, t), 2.83 (1H, m), 2.72 (2H, m), 2.43-2.18 (2H, m), 2.04 (3H, s), 1.92-1.78 (1H, m), 1.56-1.40 (6H, m), 1.38-1.23 (6H, m), 0.89 (15H, m).

Intermediate 86 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylic acid

A mixture of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylate (Intermediate 87, 0.220 g) and lithium iodide (0.055 g) in pyridine (13 mL) was irradiated in the microwave at 150° C. for 30 minutes. After cooling, the mixture was concentrated in vacuo and the residue was suspended in 1M HCl. The solid was collected by filtration and triturated with acetone then dried under vacuum to give 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydro furo[2,3-c]quinoline-6-carboxylic acid (0.190 g) as a grey solid.

¹H NMR (DMSO-d₆) δ: 13.17 (1H, s), 8.31 (1H, dd), 8.22 (1H, d), 8.02 (1H, d), 7.82 (1H, dd), 7.49 (1H, td), 7.39 (1H, d), 7.23 (1H, d).

Intermediate 87 Methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylate

A mixture of ethyl 3-[2-amino-4-(2-bromo-4-fluorobenzenesulfonylamino)-3-methoxycarbonylphenyl]-furan-2-carboxylate (Intermediate 88, 0.960 g) and potassium carbonate (0.736 g) in methanol (50 mL) was heated at reflux overnight. The resultant mixture was concentrated in vacuo and the residue was acidified with 1M HCl and extracted with a mixture of DCM and ethyl acetate. The precipitate from the acidification did not dissolve, therefore the volatiles were removed in vacuo and the aqueous slurry was filtered. The resultant paste was triturated with hot acetonitrile and the solid was collected by filtration and dried under vacuum overnight. The resultant solid was purified by chromatography on silica, eluting with a mixture of ethyl acetate and DCM, with a gradient of 0-100%, followed by methanol and DCM, with a gradient of 0-10% and finally flushing the column with methanol and DCM (50%) to give methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylate (0.685 g).

¹H NMR (DMSO-d₆) δ: 11.03 (1H, br, s), 10.48 (1H, br, s), 8.28 (1H, d), 8.17-8.10 (2H, m), 7.88 (1H, dd), 7.46 (2H, m), 7.21 (1H, d), 3.90 (3H, s).

Intermediate 88 Ethyl 3-[2-amino-4-(2-bromo-4-fluorobenzenesulfonylamino)-3-methoxycarbonylphenyl]-furan-2-carboxylate

2-Bromo-4-fluorobenzenesulfonyl chloride (0.584 g) was added to a solution of ethyl 3-(2,4-diamino-3-methoxycarbonylphenyl)-furan-2-carboxylate (Intermediate 89, 0.650 g) in DCM (30 mL) and pyridine (10 mL). The resultant mixture was stirred at room temperature for 45 minutes. A further amount of 2-bromo-4-fluorobenzene-sulfonyl chloride (0.584 g) was added and the mixture stirred for a further 1 hour. A further amount of 2-bromo-4-fluorobenzenesulfonyl chloride (0.300 g) was added and the mixture stirred for a further 30 minutes. The mixture was concentrated in vacuo and the residue was partitioned between water and DCM. The organic layer was dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was triturated with methanol and the resultant solid was collected by filtration and air dried to give ethyl 3-[2-amino-4-(2-bromo-4-fluorobenzenesulfonylamino)-3-methoxycarbonylphenyl]-furan-2-carboxylate (0.960 g) as a powder.

¹H NMR (CDCl₃) δ: 10.79 (1H, br, s), 8.25 (1H, dd), 7.62 (1H, d), 7.41 (1H, dd), 7.14 (1H, m), 7.00 (1H, d), 6.78 (1H, d), 6.49 (1H, d), 4.19 (2H, q), 3.99 (3H, s), 1.11 (3H, t).

Intermediate 89 Ethyl 3-(2,4-diamino-3-methoxycarbonylphenyl)-furan-2-carboxylate

A mixture of methyl 2,6-diamino-3-bromobenzoate (Intermediate 90, 1.0 g), 2-methoxycarbonyl-furan-3-boronic acid (0.980 g), tris-(dibenzylideneacetone)-dipalladium (0.188 g), tri-tert-butylphosphonium tetrafluoroborate (0.119 g) and cesium carbonate (4.0 g) in dioxane (45 mL) and water (6 mL) was de-gassed and flushed with argon. The resultant mixture was stirred at room temperature for 1 hour, then heated at 70° C. for 1 hour. The mixture was cooled, diluted with ethyl acetate and washed with water, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane, with a gradient of 20-50% to give ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylate (0.861 g).

¹H NMR (DMSO-d₆) δ: 7.94 (1H, d), 6.82 (1H, d), 6.65 (1H, d), 6.35 (2H, br, s), 6.00-5.91 (3H, m), 4.15 (2H, q), 3.81 (3H, s), 1.16 (3H, t).

Intermediate 90 Methyl 2,6-diamino-3-bromobenzoate

Iron powder (4.07 g) was added slowly with stirring and cooling to a solution of methyl 6-amino-3-bromo-2-nitrobenzoate (prepared according to Brock et al, Tetrahedron, 1963, 19, 1911, 2.0 g) in a mixture of absolute ethanol (49 mL), acetic acid (5 mL), formic acid (0.7 mL) and water (15 mL). On completion of the addition, the mixture was stirred at room temperature for 2 hours. The mixture was diluted with DCM and water (1:1) then filtered through Celite. The layers were separated and the aqueous layer was extracted with DCM. The combined organic layers were washed with 1M aqueous sodium hydroxide solution, dried (MgSO₄) and filtered. The filtrate was evaporated to dryness and the residue was triturated with ether and cyclohexane (1:1) and the solid was collected by filtration to give methyl 3-bromo-2,6-diaminobenzoate (1.34 g) as a pale yellow solid.

¹H NMR (CDCl₃) δ: 7.21 (1H, d), 6.11 (2H, br s), 5.88 (1H, d), 5.46 (2H, br s), 3.93 (3H, s).

Intermediate 91 Methyl 7-{2-[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate

To a suspension of methyl 7-{N-[4-fluoro-2-((Z)-3-hydroxy-prop-1-enyl)-benzenesulfonyl]-N-(methoxycarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 92, 0.150 g) in DCM (10 mL) was added N,N-di-isopropyl-N-ethylamine (0.112 g) and methanesulfonyl chloride (0.040 g). The mixture was stirred at room temperature for 15 minutes. A solution of azetidine (0.083 g) in toluene (2 mL) was added and the reaction mixture was stirred at room temperature for 1 hour. The mixture was diluted with DCM, washed with water and brine, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-10%. The resultant product was triturated with diethyl ether to give methyl 7-{2-[(Z)-3-azetidin-1-yl-prop-1-enyl]-4-fluorobenzene-sulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (0.030 g) as a white powder.

¹H NMR (CDCl₃) δ 8.02 (1H, m), 7.39 (1H, m), 7.13 (1H, d), 7.08-6.97 (2H, m), 6.91-6.83 (2H, m), 6.55 (1H, m), 5.89-5.78 (1H, m), 5.36 (2H, s), 3.87 (3H, s), 3.10 (4H, t), 2.95 (2H, dd), 1.98 (2H, m).

Intermediate 92 Methyl 7-{N-[4-fluoro-2((Z)-3-hydroxyprop-1-enyl)-benzenesulfonyl]-N-(methoxylcarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate

A mixture of methyl 7-{N-[2-bromo-4-fluorobenzenesulfonyl]-N-(methoxycarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 93, 0.200 g) and (Z)-3-tributylstannanyl-prop-2-en-1-ol (Intermediate 1, 0.230 g) in dioxane (9 mL) and water (1 mL) was de-gassed and flushed with nitrogen. tris-(Dibenzylideneacetone)dipalladium (0.034 g) and tri-tert-butylphosphonium tetrafluoroborate (0.022 g) were added and the reaction mixture was heated to 70° C. for 30 minutes. The mixture was diluted with ethyl acetate and filtered. The filtrate was washed with water, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, pre-equilibrated with ammonia solution in DCM, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-100%. The resultant product was triturated with ether to give methyl 7-{N-[4-fluoro-2((Z)-3-hydroxyprop-1-enyl)benzenesulfonyl]-N-(methoxycarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (0.150 g) as a cream powder.

¹H NMR (CDCl₃) δ: 8.19 (1H, dd), 7.46 (1H, m), 7.35 (1H, d), 7.21-7.12 (1H, m), 7.05 (1H, br, d), 7.02 (1H, d), 6.98 (1H, dd), 6.66 (1H, d), 6.10-5.99 (1H, m), 5.47 (2H, d), 4.23 (2H, m), 3.76 (3H, s), 3.66 (3H, s).

Intermediate 93 Methyl 7-{N-[2-bromo-4-fluorobenzenesulfonyl]-N-(methoxycarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate

To a suspension of sodium hydride (60% dispersion in oil, 0.043 g) in THF (10 mL) was added methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 7, 0.40 g). Once gas evolution had ceased, methyl chloroformate (0.102 mL) was added and the resultant mixture was stirred at room temperature for 2.5 hours. Saturated aqueous sodium bicarbonate solution was added and the mixture was extracted with ethyl acetate. The combined organic layers were dried (MgSO₄), filtered and the filtrate was concentrated in vacuo. The residue was triturated with ether to give methyl 7-{N[2-bromo-4-fluorobenzenesulfonyl]-N-(methoxycarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (0.230 g) as a white powder.

¹H NMR (DMSO-d₆) δ: 8.30 (1H, dd), 7.96 (1H, dd), 7.83 (1H, m), 7.61-7.53 (2H, m), 7.31 (1H, d), 7.04 (1H, d), 5.54 (2H, s), 3.77 (3H, s), 3.60 (3H, s).

Intermediate 94 Methyl 7-{4-fluoro-2-[(Z)-3-(3-acetoxyazetidin-1-yl)-prop-1-enyl]benzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate

To a solution of tert-butyl 3-acetoxyazetidine-1-carboxylate (Intermediate 95, 0.914 g) in DCM (5 mL) was added TFA (5 mL) and the mixture was stirred at room temperature for 30 minutes. The resultant mixture was concentrated in vacuo and azeotroped with toluene and diethyl ether to give acetic acid azetidin-3-yl ester trifluoroacetate salt (1.40 g) as a clear oil.

To a suspension of methyl 7-{N-[4-fluoro-2-((Z)-3-hydroxy-prop-1-enyl)-benzenesulfonyl]-N-(methoxycarbonyl)amino}-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 92, 0.220 g) in DCM (10 mL) was added N,N-di-isopropyl-N-ethylamine (1.10 g) and methanesulfonyl chloride (0.059 g). The mixture was stirred at room temperature for 1.5 hours. A solution of acetic acid azetidin-3-yl ester trifluoroacetate salt (1.40 g) in DCM (5 mL) was added and the resultant mixture was stirred at room temperature for 30 minutes. The mixture was diluted with DCM and washed with water, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of 2M ammonia in methanol and DCM, with a gradient of 0-10% to give methyl 7-{4-fluoro-2-[(Z)-3-(3-acetoxyazetidin-1-yl)-prop-1-enyl]-benzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylate (0.095 g) as a white foam.

¹H NMR (CDCl₃) δ: 8.07 (1H, dd), 7.39 (1H, m), 7.14 (1H, d), 7.11-6.96 (2H, m), 6.94-6.84 (2H, m), 6.54 (1H, d), 5.86 (1H, m), 5.37 (2H, s), 4.95 (1H, m), 3.88 (3H, s), 3.55 (2H, m), 3.05 (2H, m), 2.88 (2H, m), 1.94 (3H, s).

Intermediate 95 tert-Butyl 3-acetoxyazetidine-1-carboxylate

A solution of tert-butyl 3-hydroxyazetidine-1-carboxylate (2.0 g), DMAP (1.55 g) and triethylamine (2.34 g) in DCM (80 mL) was cooled to 0° C. A solution of acetic anhydride (2.35 g) in DCM (20 mL) was added dropwise over 20 minutes and the reaction mixture was stirred at room temperature for 1 hour. The mixture was washed with water and brine, dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was dissolved in ether and washed with 10% aqueous citric acid solution and brine, dried (MgSO₄), filtered. The filtrate was concentrated in vacuo to give tert-butyl 3-acetoxyazetidine-1-carboxylate (2.34 g) as a clear oil.

¹H NMR (CDCl₃) δ: 5.12 (1H, tt), 4.23 (2H, ddd), 3.89 (2H, dd), 2.09 (3H, s), 1.44 (9H, s).

Intermediate 96 Methyl 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate

Prepared by proceeding in a similar manner to Intermediate 53, starting from N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3) and methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 97).

¹H NMR (DMSO-d₆) δ: 7.96-7.89 (2H, m), 7.46 (1H, d), 7.21 (1H, td), 7.07 (1H, dd), 6.95 (1H, d), 6.73 (1H, d), 5.76 (1H, m), 5.19 (2H, s), 3.71 (3H, s), 3.67 (2H, br, d), 2.91 (4H, br, q), 0.96 (6H, t).

Intermediate 97 Methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate

A solution of methyl 7-bis-(tert-butoxycarbonyl)amino-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 98, 1.21 g) in formic acid (20 mL) was stirred at room temperature for 2.5 hours. The mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate and washed with aqueous potassium carbonate solution. The organic layer was dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was dissolved in pyridine (10 mL) and DCM (10 mL). 2-Bromo-4-fluorophenylsulfonyl chloride (0.821 g) was added and the reaction mixture was stirred at room temperature for 5 hours then concentrated in vacuo. The residue was dissolved in ethyl acetate, washed with 0.5M aqueous HCl solution, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with DCM. The resultant product was triturated with ether to give methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate (0.760 g) as a white solid. The filtrate from the trituration was concentrated in vacuo and purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-25%, to give a further 0.125 g of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate.

¹H NMR (CDCl₃) δ: 9.37 (1H, br, s), 8.18 (1H, dd), 7.43 (1H, dd), 7.39-7.35 (2H, m), 7.18-7.10 (2H, m), 5.27 (2H, s), 3.94 (3H, s).

Intermediate 98 Methyl 7-bis-(tert-butoxycarbonyl)amino-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate

Carbon tetrabromide (2.74 g) was added to an ice-cooled solution of methyl 6-bis-(tert-butoxycarbonyl)amino-3-(4-fluoro-2-hydroxymethylfuran-3-yl)-2-hydroxybenzoate (Intermediate 99, 1.98 g) and triphenylphosphine (2.16 g) in DCM (70 mL). The mixture was stirred for 30 minutes and then concentrated in vacuo. The residue was dissolved in acetone (80 mL) and cesium carbonate (13.4 g) was added. The reaction mixture was heated at reflux for 30 minutes, cooled and then concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate in cyclohexane, with a gradient of 0-30%. The resultant product was triturated with cyclohexane to give methyl 7-bis-(tert-butoxycarbonyl)amino-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylate (1.21 g) as a white solid.

¹H NMR (CDCl₃) δ: 7.46 (1H, dd), 7.41 (1H, d), 6.82 (1H, d), 5.33 (2H, d), 3.86 (3H, s), 1.41 (18H, s).

Intermediate 99 Methyl 6-bis-(tert-butoxycarbonyl)amino-3-(4-fluoro-2-hydroxymethylfuran-3-yl)-2-hydroxybenzoate

A solution of methyl 6-bis-(tert-butoxycarbonyl)amino-3-[2-(-tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-hydroxybenzoate (Intermediate 100, 3.66 g) in a 1M solution of tetrabutylammonium fluoride in THF (30 mL) was stirred at room temperature for 1 hour. The mixture was diluted with ethyl acetate and washed with water, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 10-50% to give methyl 6-bis-(tert-butoxycarbonyl)amino-3-(4-fluoro-2-hydroxymethylfuran-3-yl)-2-hydroxybenzoate (2.08 g) as a white solid.

¹H NMR (CDCl₃) δ: 11.97 (1H, s), 7.50 (1H, dd), 7.48 (1H, d), 6.83 (1H, d), 4.47 (2H, br, s), 3.97 (3H, s), 1.42 (18H, s).

Intermediate 100 Methyl 6-bis-(tert-butoxycarbonyl)amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-hydroxybenzoate

1M aqueous sodium hydroxide solution (25 mL) was added to a warm solution of methyl 6-bis-(tert-butoxycarbonyl)amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-(4-methylbenzenesulfonyloxy)benzoate (Intermediate 101, 5.71 g) in methanol (75 mL). The reaction mixture was stirred, while allowing it to cool to room temperature over 90 minutes. The mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was dried (Na₂SO₄), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-20% to give methyl 6-bis-(tert-butoxycarbonyl)amino-3-[2-(tert-butyldimethyl silanyloxymethyl)-4-fluoro-5-trimethylsanylfuran-3-yl]-2-hydroxybenzoate (3.66 g) as a colourless gum.

¹H NMR (CDCl₃) δ: 11.60 (1H, d), 7.48 (1H, d), 6.75 (1H, d), 4.54 (2H, s), 3.94 (3H, s), 1.39 (18H, s), 0.87 (9H, s), 0.32 (9H, s), 0.01 (6H, s).

Intermediate 101 Methyl 6-bis-(tert-butoxycarbonyl)amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-(4-methylbenznenesulfonyloxy)benzoate

A solution of methyl 6-amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-hydroxybenzoate (Intermediate 102, 3.61 g), 4-methylbenznenesulfonyl chloride (1.52 g), DMAP (0.942 g) and triethylamine (1.21 g) in DCM (40 mL) was stirred at room temperature for 16 hours. The mixture was washed with water and filtered through a phase separator. The organic layer was concentrated in vacuo and the residue was dissolved in acetonitrile (40 mL). DMAP (0.942 g) and di-tert-butyl dicarbonate (3.49 g) were added and the reaction mixture was stirred at room temperature for 2 hours. The mixture was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-20% to give methyl 6-bis-(tert-butoxycarbonyl)amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanyl-furan-3-yl]-2-(4-methylbenzenesulfonyloxy)benzoate (5.71 g) as a viscous gum.

¹H NMR (CDCl₃) δ: 7.44 (1H, dd), 7.36 (2H, d), 7.19 (1H, d), 7.09 (2H, d), 4.19 (2H, s), 3.90 (3H, s), 2.41 (3H, s), 1.41 (18H, s), 0.86 (9H, s), 0.33 (9H, s), 0.01 (6H, s).

Intermediate 102 Methyl 6-amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-hydroxybenzoate

A mixture of 2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl-boronic acid (Intermediate 103, 6.0 g), methyl 6-amino-3-bromo-2-hydroxybenzoate (prepared according to Wang et al, Bioorg Med Chem Lett 2007 17 2817, 4.27 g), tris-(dibenzylideneacetone)dipalladium (0.793 g), tri-tert-butylphosphonium tetrafluoroborate (0.502 g) and cesium carbonate (16.94 g) in dioxane (96 mL) and water (12 mL) was heated at 63° C., under an atmosphere of nitrogen for 90 minutes. The mixture was cooled and diluted with ethyl acetate, washed with water, dried (Na₂SO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-20%. The resultant product was re-purified by chromatography on silica, eluting with a mixture of DCM and cyclohexane, with a gradient of 0-100% to give methyl 6-amino-3-[2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl]-2-hydroxybenzoate (3.86 g) as a yellow oil which crystallised with scratching to give an off-white solid.

¹H NMR (CDCl₃) δ: 11.57 (1H, s), 7.20 (1H, d), 6.20 (1H, d), 5.34 (2H, br, s), 4.53 (2H, s), 4.01 (3H, s), 0.87 (9H, s), 0.31 (9H, s), 0.02 (6H, s).

Intermediate 103 2-(tert-Butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl-boronic acid

tert-Butyl-(4-fluorofuran-2-ylmethoxy)dimethylsilane (prepared according to Heffernan et al, US2008 0058395, 6.75 g) was dissolved in anhydrous THF (100 mL), under an atmosphere of nitrogen and cooled to −78° C. n-Butyllithium (2.5M in hexanes, 11.74 mL) was added and the mixture was stirred at −78° C. for 10 minutes. Chlorotrimethylsilane (3.19 g) was added and the mixture was stirred at −78° C. for 40 minutes. Further n-butyllithium (2.5M in hexanes, 11.74 mL) was added and the mixture was stirred at −78° C. for 40 minutes, before triisopropyl borate (11.04 g) was added. The resultant mixture was stirred at −78° C. for 5 minutes then allowed to warm to room temperature. 1M aqueous hydrochloric acid (100 mL) and diethyl ether (50 mL) were added and the mixture was stirred vigorously for 5 minutes. The layers were separated and the organic layer was dried (MgSO₄) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-20% to give 2-(tert-butyldimethylsilanyloxymethyl)-4-fluoro-5-trimethylsilanylfuran-3-yl-boronic acid (6.01 g) as a brown oil which was used without further characterisation.

Biological Activity

Compounds are tested for their capacity to inhibit recombinant human MetAP2 activity using the following assay.

Human recombinant MetAP2 expressed in Sf9 cells followed by affinity purification and EDTA treatment to remove endogenous active site cation was dialysed against MnCl₂ to produce the manganese enzyme used in the assay. The assay was carried out for 30 minutes at 25° C. in 50 mM HEPES buffer containing 100 mM NaCl, pH 7.5 the presence of 0.75 mM Methionine-Alanine-Serine (MAS) substrate and 50 μg/mL amino acid oxidase using a dilution of purified MetAP2 giving >3-fold signal:noise. Cleavage of the substrate by MetAP2 and oxidation of free methionine by amino acid oxidase was detected and quantified using fluorescence generated by Amplex red (10-acetyl-3,7-dihydroxyphenoxazine) in combination with horseradish peroxidase which detects H₂O₂ released during the oxidation step. The fluorescent signal was detected using a multiwell fluorimeter. Compounds were diluted in DMSO prior to addition to assay buffer, the final DMSO concentration in the assay being 1%.

The IC₅₀ is defined as the concentration at which a given compound achieves 50% inhibition of control. IC₅₀ values are calculated using the XLfit software package (version 2.0.5).

Compounds of the invention demonstrated activity in the assay of this Example as indicated in the following table, wherein A represents IC₅₀<0.1 μM, B represents IC₅₀ between 0.1 μM and 1 μM, and C represents IC₅₀>1 μM.

Compound name Activity 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A amino]-4H-furo[2,3-c]chromene-6-carboxylic acid 7-(Benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6- A carboxylic acid 8-(Benzenesulfonylmethyl)-4,5-dihydro-3,6-dioxabenzo- B [e]azulene-7-carboxylic acid 7-(Benzenesulfonylmethyl)-furo[2,3-c]quinoline-6-carboxylic B acid 7-(Benzenesulfonylmethyl)-4-oxo-4H-furo[2,3-c]chromene-6- B carboxylic acid 7-(Benzenesulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6- A carboxylic acid 8-[2-((Z)-3-Diethylamino-prop-1-enyl)-4-fluorobenzene- A sulfonyl-amino]4,5-dihydro-3,6-dioxabenzo[e]azulene-7- carboxylic acid 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzene- A sulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid 7-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonylamino]- A 4H-furo[2,3-c]chromene-6-carboxylic acid 7-[2-((Z)-3-Ethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A amino]-4H-furo[2,3-c]chromene-6-carboxylic acid 8-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonylamino]- A 4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid 7-{4-Fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzene- A sulfonyl-amino}-4H-furo[2,3-c]chromene-6-carboxylic acid 7-{4-Fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]benzene- A sulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid 7-[2-((Z)-(3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A amino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid 7-[2-((Z)-(3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A methyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid 7-[2-(3-Diethylaminopropyl)-4-fluorobenzenesulfonylamino]- A furo[2,3-c]quinoline-6-carboxylic acid 7-[2-((Z)-3-Diethylaminoprop1-enyl)-4-fluorobenzenesulfonyl- A amino]-4H-chromeno[3,4-d]isothiazole-6-carboxylic acid First eluting enantiomer of 7-[2-((Z)-(3-diethylaminoprop-1- A enyl)-4-fluorobenzenesulfonyl-methyl]-4-methyl-4H-furo[2,3- c]chromene-6-carboxylic acid Second eluting enantiomer of 7-[2-((Z)-(3-diethylaminoprop-1- B enyl)-4-fluorobenzenesulfonyl-methyl]-4-methyl-4H-furo[2,3- c]chromene-6-carboxylic acid 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-benzenesulfonylamino- A 4H-furo[2,3-c]chromene-6-carboxylic acid 7-{4-Fluoro-2-[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)-prop-1- A enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6- carboxylic acid 7-{4-Fluoro-2-[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)-prop-1- A enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6- carboxylic acid 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A amino]-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylic acid 7-{2-[(Z)-3-(Azetidin-1-yl)prop-1-enyl]-4-fluorobenzene- A sulfonyl-amino}-4H-furo[2,3-c]chromene-6-carboxylic acid 7-{4-Fluoro-2-[(Z)-3-(3-hydroxyazetidin-1-yl)-prop-1-enyl]- A benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid 7-[2-((Z)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A amino]-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylic acid 7-[2-((E)-3-Diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl- A amino]-4H-furo[2,3-c]chromene-6-carboxylic acid

INCORPORATION BY REFERENCE

All publications and patents mentioned herein, including those items listed below, are hereby incorporated by reference in their entirety for all purposes as if each individual publication or patent was specifically and individually incorporated by reference. In case of conflict, the present application, including any definitions herein, will control.

EQUIVALENTS

While specific embodiments of the subject invention have been discussed, the above specification is illustrative and not restrictive. Many variations of the invention will become apparent to those skilled in the art upon review of this specification. The full scope of the invention should be determined by reference to the claims, along with their full scope of equivalents, and the specification, along with such variations.

Unless otherwise indicated, all numbers expressing quantities of ingredients, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in this specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. 

What is claimed is:
 1. A tricyclic compound represented by:

wherein B is selected from the group consisting of:

each of which is optionally substituted on a carbon with one or two substituents each independently selected from R^(B1); D is a 6- or 7-membered heterocyclic or, heteroaryl ring; wherein B is fused to D such that the two atoms shared by D and B are both carbon; E is selected from the group consisting of: —O—C(R^(C3)R^(C4))—; —O—C(═O)—; —N(R^(N1))—C(═O)—; —N═C(R^(D2))—; and —O—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—; wherein the left hand substituent of E is attached to the phenyl ring of Formula I and the right hand substituent of E is attached to B; Y is: —C(R^(Y1)R^(Y2))— or —N(R^(Y3))—; X is selected from the group consisting of —S—, —S(═O)—, and —SO₂— with the proviso that, if Y is —N(R^(Y3))—, then X is —SO₂—; A is phenyl; R^(A1) is selected, independently for each occurrence, from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl or C₁₋₃alkoxy, wherein C₁₋₄alkyl, or C₁₋₃alkoxy may be optionally substituted by one or more halogens; n is 1 or 2; R^(A2) is hydrogen; or R^(A2) is selected from the group consisting of C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, and C₃₋₆cycloalkoxy; wherein C₁₋₆alkyl, C₂₋₆alkenyl, C₂₋₆alkynyl, C₃₋₆cycloalkyl, C₁₋₆alkoxy, C₃₋₆alkenyloxy, C₃₋₆alkynyloxy, and C₃₋₆cycloalkoxy may be optionally substituted by R^(P2), R^(B1) is selected, independently for each occurrence, from the group consisting of hydrogen, cyano, halogen, C₁₋₂alkyl or C₁₋₂alkoxy, wherein C₁₋₂alkyl or C₁₋₂alkoxy, may be optionally substituted with one or more halogens; R^(Y1) and R^(Y2) are independently selected from the group consisting of hydrogen and C₁₋₄alkyl; R^(Y3) is selected from the group consisting of hydrogen and C₁₋₄alkyl; R^(N1) is selected from the group consisting of hydrogen and C₁₋₂alkyl, wherein C₁₋₂alkyl may be optionally substituted by one or more substituents selected from halogen, cyano or hydroxyl; R^(C3) and R^(C4) are selected independently from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy and wherein C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy may be optionally substituted by one or more substituents selected from R^(P1); R^(D2) is selected from the group consisting of hydrogen, halogen, cyano, hydroxyl, C₁₋₄alkyl, C₁₋₃alkoxy, C₂₋₄alkynyl, C₂₋₄alkenyl, C₁₋₃alkyl-carbonyl-N(R^(a))— and wherein C₁₋₄alkyl, C₁₋₃alkoxy, C₂₋₄alkynyl, C₂₋₄alkenyl and C₁₋₃alkyl-carbonyl-N(R^(a))— may be optionally substituted by one or more substituents selected from R^(P1); R^(C5) and R^(C6) are selected independently from the group consisting of hydrogen, hydroxyl, cyano, halogen, C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy and wherein C₁₋₄alkyl, C₂₋₄alkenyl, C₂₋₄alkynyl or C₁₋₃alkoxy may be optionally substituted by one or more substituents selected from R^(P1); R^(a) and R^(b) are independently selected, for each occurrence, from the group consisting of hydrogen and C₁₋₄alkyl, or R^(a) and R^(b), together with the nitrogen to which they are attached, may form a 4-6 membered heterocyclic ring which may have an additional heteroatom selected from O, S, or N, and wherein C₁₋₄alkyl may be optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, oxo and hydroxyl, and wherein the 4-6 membered heterocyclic ring may be optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, oxo or hydroxyl; R^(i) and R^(j), and are selected independently for each occurrence from group consisting of hydrogen, C₁₋₄alkyl and C₃₋₆cycloalkyl optionally substituted by one or more substituents selected from R^(P1); or R^(i) and R^(j) taken together with the nitrogen to which they are attached form a 4-7 membered heterocyclyl ring which may have an additional heteroatom selected from O, S, or N, optionally substituted on carbon by one or more substituents selected from the group consisting of halogen, hydroxyl, oxo, cyano, C₁₋₆alkyl, C₁₋₆alkoxy, R^(a)R^(b)N—, R^(a)R^(b)N—SO₂—, R^(a)R^(b)N-carbonyl-, and wherein C₁₋₆alkyl or C₁₋₆alkoxy may be optionally substituted by R^(P4); or optionally substituted on nitrogen by one or more substituents selected from the group consisting of C₁₋₆alkyl, R^(a)R^(b)N-carbonyl-, and wherein C₁₋₆alkyl may be optionally substituted by R^(P4); R^(P1) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano, R^(a)R^(b)N-, R^(a)R^(b)N-carbonyl-, C₁₋₃alkoxy; R^(P2) is independently selected, for each occurrence, from the group consisting of halogen, hydroxyl, cyano, C₁₋₆alkoxy, R^(i)R^(j)N—, R^(i)R^(j)N-carbonyl-, R^(i)R^(j)N—SO₂—, R^(i)R^(j)N-carbonyl-N(R^(a))—; R^(P4) is independently selected, for each occurrence, from the group consisting of, halogen, hydroxyl, cyano; and pharmaceutically acceptable salts, stereoisomers, esters and prodrugs thereof.
 2. The tricyclic compound of claim 1, wherein B is selected from the group consisting of:


3. The tricyclic compound of claim 1, wherein B is:


4. The tricyclic compound of claim 1, wherein R^(C3), R^(C4), R^(C5), R^(C6), and R^(D2) are selected from the group consisting of: hydrogen, hydroxyl, fluorine and C₁₋₄alkyl; and R^(N1) that forms part of E is selected from hydrogen or C₁₋₂alkyl.
 5. The tricyclic compound of claim 1, wherein E is selected from the group consisting of: —O—CH₂—; —O—CH(CH₃)—; —O—C(═O)—; —N(R^(N1))—C(═O)—; —N═CH—; —CH═N—; and —O—CH₂—CH₂—.
 6. The tricyclic compound of claim 1, wherein the compound is represented by:

wherein R^(C3), R^(C4), R^(C5) and R^(C6) are independently selected from the group consisting of: hydrogen, fluorine, and C₁₋₄alkyl, wherein C₁₋₄alkyl may be optionally substituted by one or more substituents selected from the group consisting of halogen, hydroxyl, cyano, or NH₂.
 7. The tricyclic compound of claim 1, wherein Y is —N(R^(Y3))—.
 8. The tricyclic compound of claim 1, wherein X is —SO₂—.
 9. The tricyclic compound of claim 1, wherein R^(A1) is hydrogen or halogen.
 10. The tricyclic compound of claim 9, wherein R^(A1) is flourine.
 11. The tricyclic compound of claim 1, wherein R^(A2) is C₁₋₆alkyl or C₃₋₆alkenyl, wherein the C₁₋₆alkyl or the C₃₋₆alkenyl is optionally substituted by R^(i)R^(j)N—.
 12. A tricyclic compound represented by:

wherein: E is selected from the group consisting of: —O—C(R^(C3)R^(C4))—; —O—C(═O)—; —N═C(R^(D2))—; and —O—C(R^(C3)R^(C4))—C(R^(C5)R^(C6))—; Y is: —C(R^(Y1)R^(Y2))— or —N(R^(Y3))—; R^(A1) is selected from the group consisting of hydrogen and halogen; R^(A2) is hydrogen; or R^(A2) is selected from the group consisting of C₁₋₆alkyl and C₂₋₆alkenyl, each of which may be optionally substituted by R^(P2); R^(Y1) and R^(Y2) are independently selected from the group consisting of hydrogen and C₁₋₄alkyl; R^(Y3) is selected from the group consisting of hydrogen and C₁₋₄alkyl; R^(N1) is selected from the group consisting of hydrogen and C₁₋₂alkyl; R^(C3) and R^(C4) are selected independently from the group consisting of hydrogen and C₁₋₄alkyl; R^(D2) is selected from the group consisting of hydrogen and C₁₋₄alkyl; R^(C5) and R^(C6) are selected independently from the group consisting of hydrogen and C₁₋₄alkyl; R^(i) and R^(j), are selected independently for each occurrence from group consisting of hydrogen and C₁₋₄alkyl; or R^(i) and R^(j) taken together with the nitrogen to which they are attached form a 4-7 membered heterocyclyl ring which may have an additional heteroatom selected from O, S, or N, optionally substituted on carbon hydroxyl; R^(P2) is R^(i)R^(j)N—; and pharmaceutically acceptable salts, stereoisomers, esters and prodrugs thereof.
 13. The compounds: 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzene-sulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-(benzenesulfonylmethyl)-4H-furo[2,3-c]chromene-6-carboxylic acid; 8-(benzenesulfonylmethyl)-4,5-dihydro-3,6-dioxabenzo-[e]azulene-7-carboxylic acid; 7-(benzenesulfonylmethyl)-furo[2,3-c]quinoline-6-carboxylic acid; 7-(benzenesulfonylmethyl)-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-(benzene-sulfonylmethyl)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 8-[2-((Z)-3-diethylamino-prop-1-enyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid; 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonyl-amino]-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-3-ethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid; 8-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-4,5-dihydro-3,6-dioxabenzo[e]azulene-7-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzenesulfonyl-amino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-(pyrrolidin-1-yl)prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-(R)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-(3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-(S)-4-methyl-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-(3-diethylaminopropyl)-4-fluorobenzenesulfonylamino]-furo[2,3-c]quinoline-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop1-enyl)-4-fluorobenzenesulfonylamino]-4H-chromeno[3,4-d]isothiazole-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-benzenesulfonylamino-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-((R)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]-chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-((S)-3-hydroxypyrrolidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4-oxo-4,5-dihydrofuro[2,3-c]-quinoline-6-carboxylic acid; 7-{2-[(Z)-3-(azetidin-1-yl)prop-1-enyl]-4-fluorobenzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-{4-fluoro-2-[(Z)-3-(3-hydroxyazetidin-1-yl)-prop-1-enyl]-benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-1-fluoro-4H-furo[2,3-c]chromene-6-carboxylic acid; 7-[2-((E)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-4H-furo[2,3-c]chromene-6-carboxylic acid and pharmaceutically acceptable salts, stereoisomers, esters and prodrugs thereof.
 14. A pharmaceutically acceptable composition comprising a compound of claim 1 and a pharmaceutically acceptable excipient.
 15. The composition of claim 14, wherein the composition is formulated as a unit dose.
 16. The composition of claim 14, wherein the composition is formulated for oral administration.
 17. The composition of claim 14, wherein the composition is formulated for intravenous or subcutaneous administration.
 18. The tricyclic compound of claim 1, which is an isolated enantiomer of a Formula I. 